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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2036598Generated: November 3, 2026

Hydrazine hydrate (1:1) → 1-(3-Phenylbenzo[b]thiophen-2-yl)ethanamine

https://huagongshe.com/reaction/2036598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant2-(1-(3-Phenylbenzo[b]thiophen-2-yl)ethyl)isoindoline-1,3-dioneHCID 58459308—
SolventEthanolHCID 702—
Product1-(3-Phenylbenzo[b]thiophen-2-yl)ethanamineHCID 58459144—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 2-(1-(3-phenylbenzo[b]thiophen-2-yl)ethyl)isoindoline-1,3-dione (170 mg, 0.443 mmol) and hydrazine, monohydrate (0.215 mL, 4.43 mmol) in EtOH (5 mL) was heated to 50° C. overnight. After 18 h, a precipitate had developed. The precipitate was removed by filtration, rinsed with EtOH, and concentrated under reduced pressure. The concentrate was dissolved in DCM, adsorbed onto silica gel and purified by column chromatography using 10% of MeOH in DCM as eluent to give 1-(3-phenylbenzo[b]thiophen-2-yl)ethanamine as a colorless, crystalline solid: 1H NMR (400 MHz, CDCl3) δ 1.51 (d, J=6.5 Hz, 3H), 1.74 (br. s., 2H), 4.55 (q, J=6.5 Hz, 1H), 7.30-7.38 (m, 2H), 7.41-7.57 (m, 6H), 7.87-7.91 (m, 1H); LC-MS (ESI)] m/z 237.1 [M-16]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575183B2
Source datasetuspto-grants-2013_11
ORD IDord-b937be761e72487c8ac984a579cbe55f
Source noteuspto-grants-2013_11