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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047471Generated: October 27, 2026

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

https://huagongshe.com/reaction/2047471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantOxane-4-carboxylic acidHCID 219302—
SolventDimethylformamideHCID 6228—
ProductBenzyl tetrahydro-2H-pyran-4-carboxylateHCID 2313161194%

Reaction Steps

To a mixture of tetrahydro-2H-pyran-4-carboxylic acid (4.8 g) and potassium carbonate (7.6 g) and DMF (73 mL) was added dropwise benzyl bromide (4.6 mL) at 0° C. The reaction mixture was stirred at room temperature for one day, diluted with ice water, and extracted with ethyl acetate. The extract was washed with water, 0.5N hydrochloric acid, water and saturated brine, dried and concentrated under reduced pressure. The obtained residue was separated and purified by silica gel column chromatography (solvent gradient; 0→20% ethyl acetate/hexane) to give benzyl tetrahydro-2H-pyran-4-carboxylate (7.6 g, 94%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592454B2
Source datasetuspto-grants-2013_11
ORD IDord-b9e07990e8894571ab7ff17da0a066a5
Source noteuspto-grants-2013_11