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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395659Generated: November 2, 2026

Pyridine → Ethyl 6-(4-fluorophenyl)-6-oxo-5-phenoxycarbonyloxyhexanoate

https://huagongshe.com/reaction/395659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhenyl chloroformateHCID 15891—
ReactantEthyl 6-(4-fluorophenyl)-5-hydroxy-6-oxohexanoateHCID 18174685—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 6-(4-fluorophenyl)-6-oxo-5-phenoxycarbonyloxyhexanoateHCID 1817473993%

Reaction Steps

To a mixture of ethyl 6-(4-fluorophenyl)-5-hydroxy-6-oxohexanoate (13.5 g), pyridine (4.40 g) and tetrahydrofuran (100 ml) was added dropwise phenyl chlorocarbonate (8.67 g) with stirring under ice-cooling. The mixture was stirred at room temperature for 16 hours. This reaction mixture was concentrated, diluted with ethyl acetate (400 ml) and washed with water (200 ml). The organic layer was dried over anhydrous magnesium sulfate, and concentrated to give ethyl 6-(4-fluorophenyl)-6-oxo-5-phenoxycarbonyloxyhexanoate as a yellow oil (18.1 g, 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06605629B1
Source datasetuspto-grants-2003_08
ORD IDord-72aadd8b3aa94b0690a91e03ec0b92d6
Source noteuspto-grants-2003_08