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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597802Generated: November 1, 2026

Sodium hydride → HCID 18932455, compound

https://huagongshe.com/reaction/1597802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-(Bromomethyl)-1,3-benzothiazoleHCID 2776258—
ReactantMethyl (3-chloro-4-hydroxyphenyl)carbamateHCID 18932212—
SolventDimethylformamideHCID 6228—
ProductHCID 18932455HCID 1893245581.4%

Reaction Steps

44.4 mg of sodium hydride (as a 60% w/w dispersion in mineral oil) were added to a solution of 203.6 mg of methyl N-(3-chloro-4-hydroxyphenyl)carbamate [prepared as described in step (a) above] in 4 ml of dimethylformamide cooled in an ice-water bath. The resulting mixture was stirred at the same temperature for 3 minutes, and then 241.9 mg of 2-bromomethylbenzothiazole were added. The temperature of the reaction mixture was then elevated to room temperature and the mixture was stirred for 1.5 hours. At the end of this time, a saturated aqueous ammonium chloride solution was added to the reaction mixture and the resulting mixture was extracted with ethyl acetate. The resulting extract was washed consecutively with water and a saturated aqueous sodium chloride solution and then dried over anhydrous sodium sulfate. The solvent was removed by evaporation under reduced pressure to give a crude crystalline solid which was purified by column chromatography through silica gel using a 2:1 by volume mixture of hexane and ethyl acetate as the eluent, to give 286.9 mg (yield 81%) of the title compound as a solid having a melting point of 133°-135° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05736487
Source datasetuspto-grants-1998_04
ORD IDord-8ec875662a914eef9a30d70b9155f16e
Source noteuspto-grants-1998_04