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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16608Generated: October 24, 2026

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

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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantThionyl ChlorideHCID 24386—
ReactantOxane-4-carboxylic acidHCID 219302—
SolventTetrahydrofuranHCID 8028—
ProductBenzyl tetrahydro-2H-pyran-4-carboxylateHCID 2313161170.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737163B2
Source datasetuspto-grants-2010_06
ORD IDord-8fd06a8b3539453b86ef5bd3c688a452
Source noteuspto-grants-2010_06