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CAS RN: 13675-18-8 | Product Number: T2953
Tetrahydroxydiboron
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Purity:
Synonyms:
- Tetrahydroxydiborane
- Diboronic Acid
- Hypodiboric Acid
- BBA
- Bis-Boric Acid
Product Documents:
| Size | Unit Price | Saitama (Kawaguchi) | Hyogo (Amagasaki) | Stock in other WH |
Shipping Information
|
|---|---|---|---|---|---|
| 5G |
¥12,700
|
≥40 | 20 | It can be shipped in about 2 weeks after ordering | |
| 25G |
¥42,700
|
9 | 7 | It can be shipped in about 2 weeks after ordering |
* Available Stock: Prompt shipment (for products) in Saitama/Hyogo warehouse. Stock In Other WH: Shipment in about 2-3 Business Days from Saitama warehouse. Please contact us
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*TCI frequently reviews storage conditions to optimize them. Please note that the latest information on the storage temperature for the products is described on our website.
* The displayed price is the unit price and does not include consumption tax. The unit prices displayed are the latest and are subject to change without notice.
* To send your quote request for bulk quantities, please click on the "Request Bulk Quote" button. Please note that we cannot offer bulk quantities for some products.
*TCI frequently reviews storage conditions to optimize them. Please note that the latest information on the storage temperature for the products is described on our website.
Specifications
| Appearance | White to Almost white powder to crystal |
| Purity(Neutralization titration) | 98.0 to 110.0 % |
Properties (reference)
| Melting Point | 290 °C |
| Solubility (soluble in) | Methanol |
GHS
| Pictogram |
|
| Signal Word | Warning |
| Hazard Statements | H315 : Causes skin irritation. H319 : Causes serious eye irritation. |
| Precautionary Statements | P264 : Wash skin thoroughly after handling. P280 : Wear protective gloves/ eye protection/ face protection. P302 + P352 : IF ON SKIN: Wash with plenty of water. P337 + P313 : If eye irritation persists: Get medical advice/ attention. P305 + P351 + P338 : IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. P362 + P364 : Take off contaminated clothing and wash it before reuse. P332 + P313 : If skin irritation occurs: Get medical advice/ attention. |
Related Laws:
| PRTR Law (New Specific Chemical) | Class 1 Designated Chemical Substances |
Transport Information:
Application
TCI Practical Example: Chemoselective Reduction of Nitro Group Using Diboronic Acid
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Used Chemicals
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Procedure
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To a solution of trans-4-nitrostilbene (1.13 g, 5.00 mmol), diboronic acid (1.34 g, 15.0 mmol, 3.0 eq.) in DMF (30 mL) was added 4,4’-bipyridyl (3.9 mg, 0.025 mmol, 0.50 mol%) at r.t. and the mixture was stirred at the same temperature for 1 hour. The reaction mixture was diluted by 1 mol/L NaHCO3 aq. (100 mL) and the resulting solid was filtered off. The solid was purified by column chromatography (dichloromethane：hexane = 0:1 - 4:1 on silica gel) to give trans-4-aminostilbene as a yellow solid (891 mg, y. 91%).
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Experimenter’s Comments
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The reaction mixture was monitored by UPLC.
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Analytical Data
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trans-4-Aminostilbene
1H NMR (270 MHz, CDCl3); δ 7.47 (d, 2H, J = 7.0 Hz), 7.38-7.30 (m, 4H), 7.21 (t, 1H, J = 7.0 Hz), 7.03 (d, 1H, J = 15 Hz), 6.91 (d, 1H, J = 15 Hz), 6.63 (d, 2H, J = 8.6 Hz), 3.75 (brs, 2H).
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Lead Reference
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- Metal-Free, Rapid, and Highly Chemoselective Reduction of Aromatic Nitro Compounds at Room Temperature
Application
Diboronic Acid Usable for the Direct Synthesis of Aromatic Boric Acid Derivatives
[Experimental Procedure]
To an oven-dried glass vessel is added (X-Phos) palladium(II) phenethylamine chloride (7.38 mg, 0.01 mmol), X-Phos (9.52 mg, 0.02 mmol), tetrahydroxydiborane, (133.5 mg, 1.5 mmol), KOAc (294 mg, 3 mmol), and NaOt-Bu (1 mg, 0.01 mmol). The vessel is evacuated and backfilled with N2 (three times). EtOH (10 mL degassed) is added followed by the addition of 4-chloroanisole (1 mmol). The reaction is then heated to 80 °C for 18 hours. The reaction is cooled to rt then filtered through a thin pad of Celite (eluting with EtOAc) and concentrated. To the residue is added 1 M aqueous HCl and EtOAc (25 mL each). This mixture is stirred 30 min and the aqueous layer is removed, and the organic layer is washed with brine. The combined aqueous layers are extracted with EtOAc (3 x 10 mL). The combined organics are dried (Na2SO4) and then concentrated. The crude mixture is taken up in CH2Cl2, the corresponding diol is added (1.35 mmol), and the crude reaction is allowed to stir at rt. At completion of the reaction, the reaction is concentrated, and the residue is purified by flash column chromatography to afford the desired aryl boric acid derivatives.
To an oven-dried glass vessel is added (X-Phos) palladium(II) phenethylamine chloride (7.38 mg, 0.01 mmol), X-Phos (9.52 mg, 0.02 mmol), tetrahydroxydiborane, (133.5 mg, 1.5 mmol), KOAc (294 mg, 3 mmol), and NaOt-Bu (1 mg, 0.01 mmol). The vessel is evacuated and backfilled with N2 (three times). EtOH (10 mL degassed) is added followed by the addition of 4-chloroanisole (1 mmol). The reaction is then heated to 80 °C for 18 hours. The reaction is cooled to rt then filtered through a thin pad of Celite (eluting with EtOAc) and concentrated. To the residue is added 1 M aqueous HCl and EtOAc (25 mL each). This mixture is stirred 30 min and the aqueous layer is removed, and the organic layer is washed with brine. The combined aqueous layers are extracted with EtOAc (3 x 10 mL). The combined organics are dried (Na2SO4) and then concentrated. The crude mixture is taken up in CH2Cl2, the corresponding diol is added (1.35 mmol), and the crude reaction is allowed to stir at rt. At completion of the reaction, the reaction is concentrated, and the residue is purified by flash column chromatography to afford the desired aryl boric acid derivatives.
References
- 1)Palladium-Catalyzed, Direct Boronic Acid Synthesis from Aryl Chlorides: A Simplified Route to Diverse Boronate Ester Derivatives
PubMed Literature
Articles/Brochures
TCIMAIL
[TCI Practical Example] Chemoselective Reduction of Nitro Group Using Diboronic Acid[Product Highlights] Diboronic Acid Usable for the Direct Synthesis of Aromatic Boric Acid Derivatives
Product Documents (Note: Some products will not have analytical charts available.)
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Specifications
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