5-Bromo-2-mercaptobenzothiazole

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5-Bromo-2-mercaptobenzothiazole Basic information
Product Name:5-Bromo-2-mercaptobenzothiazole
Synonyms:5-Bromo-2-mercaptobenzothiazole;5-CHLORO-BENZOTHIAZOLE-2-THIOL;TIMTEC-BB SBB005398;5-BROMO-2-MERCAPTO BENZOTHLAZOLE;5-Bromo-2-Thiobenzothiazole;5-BROMO-2-MERCAPTO BENZIMIDAZOLE;5-broMo-1,3-benzothiazole-2-thiol;5-Bromobenzo[d]thiazole-2(3H)-thione
CAS:71216-20-1
MF:C7H4BrNS2
MW:246.15
EINECS:226-235-0
Product Categories:Heterocycles;Heterocyclic Compound
Mol File:71216-20-1.mol
5-Bromo-2-mercaptobenzothiazole Structure
5-Bromo-2-mercaptobenzothiazole Chemical Properties
Melting point 198-200 °C(lit.)
storage temp. 2-8°C
AppearanceYellow to brown Solid
CAS DataBase Reference71216-20-1(CAS DataBase Reference)
Safety Information
Hazard Codes Xn
Risk Statements 36/37/38-20/21/22
Safety Statements 36/37/39-26-22
WGK Germany 3
RTECS DL6490000
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
5-Bromo-2-mercaptobenzothiazole Usage And Synthesis
Chemical PropertiesYellow solid
Synthesis
5-Bromobenzothiazole

768-11-6

5-Bromo-2-mercaptobenzothiazole

71216-20-1

General procedure for the synthesis of 5-bromo-2-mercaptobenzothiazole from 5-bromobenzothiazole: 5-bromobenzothiazole (214.08 mg, 1.0 mmol), 1,3-propanedithiol (325 μL, 3.0 mmol), potassium carbonate (552 mg, 4.0 mmol), and DMSO (2 mL) were added into a reaction tube equipped with a magnetic stirrer. The reaction system was displaced three times with nitrogen to remove air, followed by stirring the reaction for 12 h in an oil bath at 120 °C. Upon completion of the reaction, the reaction mixture was transferred to a dispensing funnel and washed with an appropriate amount of water. The pH of the aqueous phase was adjusted to 1-3 with dilute hydrochloric acid, followed by extraction of the organic phase with dichloromethane. The organic phases were combined and dried with anhydrous magnesium sulfate. After filtration, the organic phase was concentrated under reduced pressure and the resulting crude product was purified by column chromatography to give a pink solid product (112.4 mg, 45.7% yield).

References[1] Patent: CN108530374, 2018, A. Location in patent: Paragraph 0032; 0033
5-Bromo-2-mercaptobenzothiazole Preparation Products And Raw materials
Raw materials5-Bromobenzothiazole-->5-Bromo-2-fluoroaniline-->Potassium ethylxanthate-->1,3-Dimercaptopropane-->Dimethyl sulfoxide-->Potassium carbonate
Tag:5-Bromo-2-mercaptobenzothiazole(71216-20-1) Related Product Information
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