Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1729172Generated: November 1, 2026

2-(methylamino)benzenethiol → HCID 15027933, compound

https://huagongshe.com/reaction/1729172

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(methylamino)benzenethiolHCID 452161—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 15027913HCID 15027913—
CatalystBenzyl triethylammonium chlorideHCID 66133—
SolventChloroformHCID 6212—
ProductHCID 15027933HCID 15027933—

Reaction Conditions

Temperature5 °C

Reaction Steps

4.5 g (=0.032 m) of 2-(methylamino)-thiophenol, 6 g of triethylbenzylammonium chloride, and 11.20 g of sodium hydrogen carbonate were added to 120 ml of chloroform. The resulting suspension was cooled to 5° C., and then a solution of 10.88 g of 2,6-dibromohexanoyl bromide in 20 ml of chloroform was added dropwise so slowly that the temperature did not exceed 5° C. 20 minutes were required for the addition. The reaction mixture was then allowed to warm to room temperature and was subsequently heated under reflux for 4 hours. The reaction mixture was worked up by cooling and filtering it. The chloroform phase was washed, dried over sodium sulfate, and the solvent was distilled off. The 2-(4-bromobutyl)-4-methyl-2H-1,4-benzothiazine-3(4H)-one which formed was isolated from the remaining residue by fractional column chromatography. 2.78 g of white crystals having a melting point of 116° C. were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05332733
Source datasetuspto-grants-1994_07
ORD IDord-50aeeaf9ee8b401b9400658386da7065
Source noteuspto-grants-1994_07