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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747454Generated: October 30, 2026

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

https://huagongshe.com/reaction/747454

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 numberUS07396848B1
Source datasetuspto-grants-2008_07
ORD IDord-dd4fa991b13d450f9b004234f64b1eba
Source noteuspto-grants-2008_07