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CAS RN: 1314538-55-0 | Product Number: P2155
Potassium [[(tert-Butoxycarbonyl)amino]methyl]trifluoroborate
Purity: >97.0%(N)
Synonyms:
- Potassium (N-Boc-aminomethyl)trifluoroborate
Product Documents:
Size | Unit Price | Same Day | 2-3 Business Days | Other Lead Time | Shipping Information |
---|---|---|---|---|---|
1G |
$215.00
|
25 | 16 | Contact Us | |
5G |
$723.00
|
≥60 | 11 | Contact Us |
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Product Number | P2155 |
Purity / Analysis Method | >97.0%(N) |
Molecular Formula / Molecular Weight | C__6H__1__2BF__3KNO__2 = 237.07 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
Packaging and Container | 1G-Glass Bottle with Plastic Insert (View image) |
CAS RN | 1314538-55-0 |
Reaxys Registry Number | 21751374 |
PubChem Substance ID | 253661860 |
MDL Number | MFCD19686142 |
Specifications
Appearance | White to Almost white powder to crystal |
Purity(with Total Nitrogen) | min. 97.0 % |
NMR | confirm to structure |
Properties (reference)
Melting Point | 181 °C |
Solubility in water | Slightly soluble |
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:
Transport Information:
H.S.code* | 2931.90-000 |
Application
Introduction of an aminomethyl group by Suzuki-Miyaura cross-coupling reaction
General Procedure for the Suzuki?Miyaura Cross-coupling Reaction: A sealed tube is charged with potassium (tert-butoxycarbonyl)amino)methyl)trifluoroborate (62 mg, 0.263 mmol, 1.05 equiv), an aryl or heteroaryl chloride (0.25 mmol, 1.0 equiv), Pd(OAc)2 (3 mg, 0.013 mmol, 0.05 equiv), SPhos ligand (0.03 mmol, 0.1 equiv) and K2CO3 (104 mg, 0.75 mmol, 3.0 equiv). The mixture is then purged with argon. Toluene/H2O (4:1, 0.8 mL / 0.2 mL) is then added to the reaction tube. The reaction mixture is stirred for 22 h at 85 °C and then cooled to rt. A solution of pH 7 buffer (2 mL) is added, and the resulting mixture is extracted with EtOAc (2 × 3 mL). The organic layer is combined, dried (MgSO4) and filtered. The solvent is removed in vacuo and the product is purified by column chromatography to give the corresponding compound in shown yield.
References
- Synthesis and Suzuki–Miyaura Cross-Coupling Reactions of Potassium Boc-Protected Aminomethyltrifluoroborate with Aryl and Hetaryl Halides
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