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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788381Generated: November 2, 2026

Water → HCID 57602810, compound

https://huagongshe.com/reaction/1788381

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTetrahydro-4H-pyran-4-oneHCID 121599—
ReactantTriethyl 2-fluoro-2-phosphonoacetateHCID 2734865—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 57602810HCID 5760281088.8%

Reaction Steps

Into a cooled (−10° C.) solution of 5.25 g (21.68 mmol) of 2-fluoro-2-phosphonoacetic acid triethyl ester in tetrahydrofuran (30 mL) under an atmosphere of argon was dropped 13.2 mL (19.87 mmol) of 1.5 mol/L n-butyllithium in hexane (available from KANTO KAGAKU). After stirring for 20 minutes at room temperature, 2.0 g (19.87 mmol) of tetrahydropyran-4-one was dropped thereto and stirred for 2 hours at about 55° C. The obtained mixture was left to cool to room temperature and then poured into water, followed by extraction with ether. The ether extract was washed with water (three times) and saturated brine and dried over anhydrous magnesium sulfate, and the solvent was removed. The obtained residue was purified by medium pressure liquid column chromatography on silica gel (developing solvent: hexane-ethyl acetate) to obtain 3.32 g (yield 88.8%) of fluoro-(tetrahydropyran-4-ylidene)acetic acid ethyl ester (IX-16) as colorless liquid. Its physical property is shown blow.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07511144B2
Source datasetuspto-grants-2009_03
ORD IDord-f0c4cdd380964b5f8fd335b8114b5110
Source noteuspto-grants-2009_03