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6-Fluoro-benzothiazole-2-thiol

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Company Name: Energy Chemical  
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6-Fluoro-benzothiazole-2-thiol manufacturers

6-Fluoro-benzothiazole-2-thiol Basic information
Product Name:6-Fluoro-benzothiazole-2-thiol
Synonyms:6-FLUORO-BENZOTHIAZOLE-2-THIOL;2(3H)-Benzothiazolethione,6-fluoro-(9CI);6-Fluorobenzo[d]thiazole-2(3H)-thione;6-Fluoro-1,3-benzothiazole-2-thiol, 6-Fluoro-2-mercaptobenzo[d]thiazole;6-Fluoro-2-sulphanyl-1,3-benzothiazole;6-fluoro-3H-1,3-benzothiazole-2-thione;2-Mercapto-6-fluorobenzothiazole;2(3H)-Benzothiazolethione, 6-fluoro-
CAS:80087-71-4
MF:C7H4FNS2
MW:185.24
EINECS:
Product Categories:BENZOTHIAZOLE
Mol File:80087-71-4.mol
6-Fluoro-benzothiazole-2-thiol Structure
6-Fluoro-benzothiazole-2-thiol Chemical Properties
Melting point 225-227 °C(Solv: chloroform (67-66-3); ligroine (8032-32-4))
Boiling point 304.4±44.0 °C(Predicted)
density 1.55±0.1 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka9.30±0.20(Predicted)
AppearanceWhite to off-white Solid
Safety Information
HS Code 2934208090
MSDS Information
6-Fluoro-benzothiazole-2-thiol Usage And Synthesis
Synthesis
Carbon disulfide

75-15-0

4-Fluoro-2-iodoaniline

61272-76-2

6-Fluoro-benzothiazole-2-thiol

80087-71-4

At room temperature and under the protection of argon, 2-iodo-4-fluoroaniline (2 mmol), carbon disulfide (10 mmol), sodium sulfide (4 mmol), and N,N-dimethylformamide (2 mL) were sequentially added to a 50 mL sealed reaction tube, and the air inside the reaction tube was replaced three times with argon. The reaction tube was sealed and placed in an oil bath at 110°C with electromagnetic stirring for 12 hours. The reaction process was monitored by thin layer chromatography (TLC, silica gel plate). Upon completion of the reaction, the reaction mixture was cooled to room temperature, 3 mol/L hydrochloric acid (2 mL) was added slowly and stirring was continued for 30 min. Subsequently, the reaction mixture was extracted with dichloromethane (3 x 20 mL), the organic phases were combined and dried with anhydrous magnesium sulfate. After the solvent was removed by concentration under reduced pressure, the residue was purified by silica gel column chromatography (eluent: petroleum ether/ethyl acetate gradient elution) to afford the target compound 6-fluoro-2-mercaptobenzothiazole.

References[1] Organic Letters, 2011, vol. 13, # 12, p. 3202 - 3205
[2] Synthetic Communications, 2017, vol. 47, # 20, p. 1916 - 1925
[3] Patent: CN104098529, 2016, B. Location in patent: Paragraph 0040-0041
6-Fluoro-benzothiazole-2-thiol Preparation Products And Raw materials
Raw materials2,4-Difluoroaniline-->Carbon disulfide-->4-Fluoro-2-iodoaniline-->Potassium ethylxanthate-->N,N-Dimethylformamide-->Sodium sulfide nonahydrate
Tag:6-Fluoro-benzothiazole-2-thiol(80087-71-4) Related Product Information
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