戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 130855作成日:2026年10月24日

Benzo[b]thiophene-3-acetonitrile → Benzo[b]thiophene-3-ethanamine

https://huagongshe.com/ja/reaction/130855

反応式

関与物質

役割名称HCID仕込み量
反応物Benzo[b]thiophene-3-acetonitrileHCID 76681—
反応物Aluminium lithium hydrideHCID 21226445—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物Benzo[b]thiophene-3-ethanamineHCID 2674324.4%

反応手順

Reduce benzo[b]thiophen-3-yl-acetonitrile (350.9 mg, 2.0 mmol) in Et2O (6.0 mL) with 1.0 M LAH in THF (6.0 mL) at 0-10° C. for 1 hour. Carry out Fieser work-up to remove the LAH. Concentrate and pass through an SCX column, washing with MeOH and then eluting with 2.0 M NH3 in MeOH. Concentrate the eluant and purify twice by chromatography, eluting with 75:20:5 EtOAc/hexanes/2.0 M NH3 in MeOH and then with 70:20:10 EtOAc/hexanes/2.0 M NH3 in MeOH to yield the title compound (86.5 mg, 24%): MS ES+ 178.2 (M+H)+, 161.2 (base peak); 1H NMR (DMSO-d6) δ 7.94 (d, J=7.3 Hz, 1H), 7.81 (d, J=7.8 Hz, 1H), 7.40-7.33 (m, 3H), 3.32 (br s, 2H), 2.88 (br s, 4H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07381719B2
出典データセットuspto-grants-2008_06
ORD IDord-14dacf88aad24b3c997e962a88d7be9e
出典メモuspto-grants-2008_06