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HRID 16608作成日:2026年10月23日

Benzyl Alcohol → Benzyl tetrahydro-2H-pyran-4-carboxylate

https://huagongshe.com/ja/reaction/16608

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl AlcoholHCID 244—
反応物Thionyl ChlorideHCID 24386—
反応物Oxane-4-carboxylic acidHCID 219302—
溶媒TetrahydrofuranHCID 8028—
生成物Benzyl tetrahydro-2H-pyran-4-carboxylateHCID 2313161170.1%

反応条件

温度60 °C

反応手順

A mixture of tetrahydropyran-4-yl-carboxylic acid (910 mg, 6.99 mmol) and SOCl2 (5.0 mL) was stirred for 1 h at 60° C. and concentrated in vacuo. To the residue were added benzyl alcohol (1.52 g, 14.1 mmol) and tetrahydrofuran (5.0 mL) at ambient temperature. The resulting mixture was stirred for 13 h at ambient temperature and concentrated in vacuo. The residue was purified by preparative thin layer chromatography (silica gel, eluting with hexane/ethyl acetate (2:1)) to give 1.08 g (70%) of the title compound as a pale yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737163B2
出典データセットuspto-grants-2010_06
ORD IDord-8fd06a8b3539453b86ef5bd3c688a452
出典メモuspto-grants-2010_06