戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1248790作成日:2026年10月25日

Benzene, 1-(chloromethyl)-2-fluoro- → N-(2-Fluorophenylmethyl)-3-hydroxy-3-phenylpropylamine

https://huagongshe.com/reaction/1248790

反応式

関与物質

役割名称HCID仕込み量
反応物Benzene, 1-(chloromethyl)-2-fluoro-HCID 9580—
反応物2,2,6,6-TetramethylpiperidineHCID 13035—
反応物3-Amino-1-phenylpropan-1-olHCID 121548—
溶媒AcetonitrileHCID 6342—
生成物N-(2-Fluorophenylmethyl)-3-hydroxy-3-phenylpropylamineHCID 1295184152.5%

反応手順

A mixture of 3-hydroxy-3-phenylpropylamine (7.0 g, 46 mM) and 2,2,6,6-tetramethylpiperidine (7.9 ml, 46 mM) in acetonitrile (100 ml) was treated with a solution of o-fluorobenzyl chloride (6.75 g, 46 mM) in acetonitrile (10 ml). After 24 hours the resulting precipitate was removed by filtration and washed with acetonitrile (2×10 ml). The combined filtrate and washings were evaporated under reduced pressure and the residue partitioned between 2N hydrochloric acid (50 ml) and ether (100 ml). The aqueous layer was basified and extracted with ether, the ether extracts dried and evaporated. Chromatography on Grade 3 silica using 2% methanol in chloroform as eluant followed by distillation gave the title compound (6.3 g) b.p. 156°-160° C. (0.2 mbar).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04626522
出典データセットuspto-grants-1986_12
ORD IDord-868acbd05e6a4849a9c7572a5f4568ed
出典メモuspto-grants-1986_12