戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 330268作成日:2026年10月26日

1-Chloro-3,4-dihydronaphthalene-2-carboxaldehyde → (1-Chloro-3,4-dihydronaphthalen-2-yl)methanol

https://huagongshe.com/reaction/330268

反応式

関与物質

役割名称HCID仕込み量
反応物1-Chloro-3,4-dihydronaphthalene-2-carboxaldehydeHCID 76752—
反応物Sodium borohydrideHCID 4311764—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
生成物(1-Chloro-3,4-dihydronaphthalen-2-yl)methanolHCID 14819335102.2%

反応手順

To a mixture of sodium borohydride (2.83 g, 0.075 mol) in methanol (150 mL) at 0° C., was added dropwise a solution of 1-chloro-2-formyl-3,4-dihydronaphthalene (9.59 g, 0.05 mol) in dry THF (150 mL). The reaction was stirred at room temperature for 1 hour, carbon dioxide was cautiously bubbled through the reaction mixture for 15 minutes, and the resulting mixture was concentrated under reduced pressure. The residue was diluted with water (150 mL), extracted with ether (3×150 mL), dried (MgSO4) and concentrated to give 9.95 g (102%) of product as a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04895860
出典データセットuspto-grants-1990_01
ORD IDord-a203c78374d04dca998de492e3dae3ff
出典メモuspto-grants-1990_01