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CAS RN: 503596-47-2 | Product Number: T3773
(Triphenylmethyl)thionyl Imide
Purity: >97.0%(GC)
Synonyms:
- Tritylthionyl Imide
- TrNSO
Product Documents:
Size | Unit Price | Shanghai | Tianjin | Japan* |
---|---|---|---|---|
1G |
¥470.00
|
14 | 1 | 32 |
5G |
¥1,610.00
|
≥40 | 1 | ≥40 |
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Product Number | T3773 |
Purity / Analysis Method | >97.0%(GC) |
Molecular Formula / Molecular Weight | C__1__9H__1__5NOS = 305.40 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
Store Under Inert Gas | Store under inert gas |
Condition to Avoid | Air Sensitive |
Packaging and Container | 1G-Glass Bottle with Plastic Insert (View image) |
CAS RN | 503596-47-2 |
PubChem Substance ID | 468592935 |
Specifications
Appearance | White to Light yellow powder to crystal |
Purity(GC) | min. 97.0 % |
Melting point | 96.0 to 100.0 °C |
Properties (reference)
Melting Point | 98 °C |
GHS
Related Laws:
Transport Information:
Customs Control Conditions (Q) |
Application
TrNSO : A Versatile sulfonimidoylating agent
TrNSO (50.0 mg, 0.164 mmol) is dissolved in THF (1 mL). The reaction is cooled to 0 °C. Grignard reagent (0.164 mmol, 1.0 eq.) is added dropwise and the mixture is stirred for 5 min. Tert-butyl hypochlorite (19.5 μL, 0.172 mmol, 1.05 eq.) is added in the dark and the mixture is stirred for 15 min prior to addition of triethylamine (23 μL, 0.164 mmol, 1.0 eq.) and the corresponding amine (1.0-1.2 eq.). The reaction mixture is stirred at room temperature for 16 h. Methanesulfonic acid (53 μL, 0.819 mmol, 5.0 eq.) is added and the reaction is stirred vigorously for 15 min at room temperature before dilution with CH2Cl2. The solution is washed with saturated aqueous sodium bicarbonate solution, then the layers are separated and the aqueous phase is extracted with CH2Cl2 × 3 times. The combined organic layers are concentrated in vacuo. Purification by silica gel flash chromatography affords the desired sulfonimidamide.
References
- One-Pot, Three-Component Sulfonimidamide Synthesis Exploiting the Sulfinylamine Reagent N-Sulfinyltritylamine, TrNSO
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