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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236782Generated: October 30, 2026

Water → 3-Ethylamino-2-phenyl-benzo(b)thiophene

https://huagongshe.com/reaction/236782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDichloromethaneHCID 6344—
ReactantHCID 15700627HCID 15700627—
ReactantAluminium lithium hydrideHCID 21226445—
Solvent1,4-DioxaneHCID 31275—
Product3-Ethylamino-2-phenyl-benzo(b)thiopheneHCID 15700631—

Reaction Steps

10.7 g (40 mmol) of 3-acetamido-2-phenyl-benzo(b)thiophene and 3.8 g (0.1 mol) of LiAlH4 in 200 milliliters of absolute dioxan is refluxed with stirring for 1 hour. The cooled reaction mixture is mixed with water to decompose the excess LiAlH4 and, after the addition of 300 milliliters of CH2Cl2, it is stirred for a further 15 minutes. After centrifuging with the addition of hyflo, the organic phase is dried over potassium carbonate and evaporated: 3-ethylamino-2-phenyl-benzo(b)thiophene in the form of a crude oily product. It is dissolved in a little chloroform and converted into the hydrochloride by hydrochloric gas: 10.9 g (94% of theory) of colourless sticks in ethanol, decomposition from 205° C. (in sealed tube).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04157399
Source datasetuspto-grants-1979_06
ORD IDord-70da6258de8946ba9e609423515c86d5
Source noteuspto-grants-1979_06