Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597786Generated: October 30, 2026

Ammonium Chloride → 1-(1,3-Benzothiazol-2-yl)ethan-1-ol

https://huagongshe.com/reaction/1597786

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1,3-Benzothiazole-2-carbaldehydeHCID 241608—
ReactantHCID 178418573HCID 178418573—
Product1-(1,3-Benzothiazol-2-yl)ethan-1-olHCID 283067466%

Reaction Steps

5.0 ml of methylmagnesium bromide were added dropwise to a solution of 0.61 g of 2-formylbenzothiazole [prepared as described in step (a) above] which was cooled in an acetone-dry ice bath. The reaction vessel was transferred to an ice-water bath and the reaction mixture was stirred for 3.5 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 with a saturated aqueous sodium chloride solution and then dried over anhydrous sodium sulfate. The solvent was then removed by evaporation under reduced pressure and the resulting residue was purified by column chromatography through silica gel using a 4:1 by volume mixture of hexane and ethyl acetate as the eluent, to give 0.44 g (yield 66%) of the title compound as a solid having a melting point of 59° to 60° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05736487
Source datasetuspto-grants-1998_04
ORD IDord-f4359b0c2eed4677a40be68d6992f6bb
Source noteuspto-grants-1998_04