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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 418756Generated: October 30, 2026

Benzyl Alcohol → Benzyl 2-(tetrahydro-2H-pyran-4-yl)acetate

https://huagongshe.com/reaction/418756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantTriethylamineHCID 8471—
ReactantTetrahydropyran-4-ylacetic acidHCID 2773575—
ReactantEthyl acetate hexaneHCID 21226206—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductBenzyl 2-(tetrahydro-2H-pyran-4-yl)acetateHCID 5970653332.5%

Reaction Steps

To a solution of 2-(tetrahydropyran-4-yl)acetic acid (325 mg, 2.26 mmol) in anhydrous dichloromethane (10 mL) were added benzyl alcohol (439 mg, 2.94 mmol), 1-ethyl-3-(3-dimethylammoniumpropyl)carbodiimide hydrochloride (564 mg, 2.94 mmol) and triethylamine (297 mg, 2.94 mmol) at room temperature, and the mixture was stirred for 12 h. The reaction mixture was diluted with water (1 mL) to separate the phases, and the organic layer was further washed with water (1 mL) and brine (1 mL). The organic layer was concentrated under reduced pressure, and the residue thus obtained was subjected to silica gel column chromatography (hexane-ethyl acetate 7:1) to give 172 mg of the title compound as oil (yield: 32%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093294B2
Source datasetuspto-grants-2012_01
ORD IDord-6ef58ff63fdd4c5588d883b79c2d4e1f
Source noteuspto-grants-2012_01