Benzenecarbothioic acid, S-(trifluoromethyl) ester

Benzenecarbothioic acid, S-(trifluoromethyl) ester Suppliers list
Company Name: Shandong Territorial sea Biological Technology Co., LTD  
Tel: 15092083467
Email: 18660263263@163.com
Products Intro: Product Name:S-(Trifluoromethyl) benzothioate
CAS:175400-81-4
Purity:97+% Package:1g;5g;10g;25g;50g;100g;250g;500g;按需分装
Company Name: Ningbo Chemrio Chemtech Co,.Ltd.  
Tel: 0574-27891269 18667892864
Email: frank.xiaodong@chemriotech.com
Products Intro: Product Name:S-(trifluoromethyl) benzothioate
CAS:175400-81-4
Purity:98% Package:25KG;5KG;1KG
Benzenecarbothioic acid, S-(trifluoromethyl) ester Basic information
Product Name:Benzenecarbothioic acid, S-(trifluoromethyl) ester
Synonyms:Benzenecarbothioic acid, S-(trifluoromethyl) ester;S-(trifluoromethyl) benzothioate
CAS:175400-81-4
MF:C8H5F3OS
MW:206.18
EINECS:
Product Categories:
Mol File:175400-81-4.mol
Benzenecarbothioic acid, S-(trifluoromethyl) ester Structure
Benzenecarbothioic acid, S-(trifluoromethyl) ester Chemical Properties
Safety Information
MSDS Information
Benzenecarbothioic acid, S-(trifluoromethyl) ester Usage And Synthesis
Chemical PropertiesS-(Trifluoromethyl)benzothioate (TFBT) has been developed as an inexpensive, bench-stable, and user-friendly trifluoromethylthiolation reagent, which can be easily synthesized by using KF as the only fluorine source.
SynthesisUnder the protection of nitrogen, potassium fluoride (23.2 g, 400 mmol, 4.0 equiv), 18-c-6 (31.8 g, 120 mmol, 1.2 equiv) and acetonitrile (200 mL) were added to a dry Schlenk tube. After cooling to  15°C, thiophosgene (9.2 mL, 120 mmol, 1.2 equiv) was added, and the mixture was vigorously stirred for 4 h. Then, the temperature was cooled to  30°C and benzoyl chloride (11.6 mL, 100 mmol, 1.0 equiv) added. After stirring for another 2 h, the reaction was quenched by water, raised to room temperature, and extracted with ether (3×100 mL). The organic phases were combined, washed with water and saturated brine, and dried with anhydrous Na2SO4. After filtration, the solution was concentrated by evaporation and the residue was distilled under reduced pressure (8 Torr, 70–80°C) to provide Benzenecarbothioic acid, S-(trifluoromethyl) ester as a yellow liquid (12.6 g, 61%).
References[1] DEPEI MENG. S-(Trifluoromethyl)Benzothioate (TFBT): A KF-Based Reagent for Nucleophilic Trifluoromethylthiolation[J]. Chemistry - A European Journal, 2022, 28 13. DOI:10.1002/chem.202104395.
Benzenecarbothioic acid, S-(trifluoromethyl) ester Preparation Products And Raw materials
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