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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164141Generated: October 31, 2026

Hydrochloric Acid → HCID 12412186, compound

https://huagongshe.com/reaction/2164141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22750359HCID 22750359—
SolventChloroformHCID 6212—
ProductHCID 12412186HCID 12412186—

Reaction Steps

To a suspension of 15.5 parts by weight of 2-phenylbenzo[b]thiophene-3-acetonitrile in a solution of 29.6 parts by weight of cobaltous chloride hexahydrate in 769 parts by volume of methanol-benzene (5:1) is added slowly 23.8 parts by weight of sodium borohydride at 0° C. After the addition is completed, the mixture is allowed to warm to room temperature and stirred for 72 hours. The reaction mixture is then partitioned between water and ether. The aqueous layer is separated, basified with concentrated ammonium hydroxide and extracted (3xs) with ether. The organic fractions are combined, dried and concentrated to afford crude 2-phenylbenzo[b]thiophene-3-ethanamine. This material is dissolved in chloroform and shaken with 100 parts by volume of 10% aqueous hydrochloric acid. A solid precipitates; filtration of this material affords 2-phenylbenzo[b]thiophene-3-ethanamine hydrochloride, melting at 200°-201° C. (decomposition). This compound is represented by the following stuctural formula. ##STR28##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04137414
Source datasetuspto-grants-1979_01
ORD IDord-c77c21e7d4b24732b998bb93c1d16fb7
Source noteuspto-grants-1979_01