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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458425Generated: October 29, 2026

Allyl Alcohol → Allyl 4-(4-fluorophenyl)-3-oxobutanoate

https://huagongshe.com/reaction/458425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl AlcoholHCID 7858—
Reactant2-(4-Fluorophenyl)acetic acidHCID 9837—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductAllyl 4-(4-fluorophenyl)-3-oxobutanoateHCID 1844198895%

Reaction Steps

To a CH2Cl2 (210 mL) solution of 4-fluorophenyl acetic acid (32.28 g, 209.42 mmol) at 0° C. was added DMAP (25.58 g, 209.42 mmol), and Meldrum's Acid (30.18 g, 209.42 mmol) followed by DCC (43.21 g, 209.42 mmol). The reaction mixture was warmed to ambient temperature and stirred for 4 h. The reaction was filtered to remove the DCU and the filtrate washed with 1N HCl, H2O, and brine. The organics were dried (Na2SO4), filtered and concentrated to a yellow oil. The residue was redissolved in THF (200 mL) and allyl alcohol (14.38 mL, 211.51 mmol). The reaction mixture was refluxed for 3 h and then concentrated to deliver 47 g (95% yield) of the title compound as a pale yellow oil and used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07189851B2
Source datasetuspto-grants-2007_03
ORD IDord-972165515bc042b7b365ec30344c51e0
Source noteuspto-grants-2007_03