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HRID 1976554作成日:2026年10月24日

Benzyl Chloride → 3-(Benzyloxy)-4-methoxybenzyl alcohol

https://huagongshe.com/ja/reaction/1976554

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl ChlorideHCID 7503—
反応物3-Hydroxy-4-methoxybenzyl alcoholHCID 78089—
反応物Potassium tert-butoxideHCID 23665647—
溶媒1-PropanolHCID 1031—
生成物3-(Benzyloxy)-4-methoxybenzyl alcoholHCID 7462288.2%

反応手順

A solution of 3-hydroxy-4-methoxy-benzyl alcohol (61.67 g, 400 mmole) in 1-propanol (600 ml) was treated at 60° C. with 97% t-BuOK (55.52 g, 480 mmole), at 90° C. with benzyl chloride (66.57 ml, 560 mmole) and the resulting mixture heated under reflux for 2 hours. Then at 90° C. a second batch of t-BuOK (9.25 g, 80 mmole) was added. After a further hour at reflux a third batch of t-BuOK (9.25 g, 80 mmol) and a second batch of benzyl chloride (9.51 ml, 80 mmole) was added at 90° C. After a further 2.5 hours at reflux the mixture was cooled to room temperature and the solid filtered off. The solvents were removed in vacuo, the residue treated with water (300 ml) and one-third of the solvent removed in vacuo. Water (100 ml) was added to the residue, which was then distilled off in vacuo and the procedure repeated. The resulting suspension was filtered, the solid was collected, dried and triturated with petroleum ether (2×600 ml) to give 3-benzyloxy-4-methoxy-benzyl alcohol, (86.21 g, 88.2%) mp 62-65° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06228859B1
出典データセットuspto-grants-2001_05
ORD IDord-3dcb48659071488e86420061ef5104b4
出典メモuspto-grants-2001_05