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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341678Generated: October 31, 2026

Triethylamine → 2,2-dimethyl propionic acid 4-(3-ethyl-4'-fluorobiphenyl-4-yl)-2,2,6-trimethyl-5-oxo-5,6-dihydro-2H pyran-3-yl ester

https://huagongshe.com/reaction/341678

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPivaloyl chlorideHCID 62493—
Reactant4-(3-Ethyl-4'-fluorobiphenyl-4-yl)-2,2,6-trimethylpyran-3,5-dioneHCID 68732340—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2,2-dimethyl propionic acid 4-(3-ethyl-4'-fluorobiphenyl-4-yl)-2,2,6-trimethyl-5-oxo-5,6-dihydro-2H pyran-3-yl esterHCID 5956258584.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-(3-ethyl-4′-fluoro-biphenyl-4-yl)-2,2,6-trimethylpyran-3,5-dione (0.125 g, 0.35 mmol) in dichloromethane (5 ml) is added triethylamine (0.2 ml, 1.43 mmol) and the reaction mixture is cooled to 0° C. Pivaloyl chloride (0.2 ml, 1.63 mmol) is added slowly at 0° C. and the mixture is stirred at 0° C. for 5 hours. The reaction mixture is diluted with water and extracted with dichloromethane (3×25 ml). The organic extracts are combined, dried over anhydrous sodium sulphate and concentrated under reduced pressure. The residue is purified by column chromatography on silica gel to afford 2,2-dimethyl propionic acid 4-(3-ethyl-4′-fluorobiphenyl-4-yl)-2,2,6-trimethyl-5-oxo-5,6-dihydro-2H pyran-3-yl ester (130 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895761B2
Source datasetuspto-grants-2014_11
ORD IDord-4d1afe52bf854891b820c700c8ee40ac
Source noteuspto-grants-2014_11