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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158139Generated: November 4, 2026

Triethylamine → HCID 59512572, compound

https://huagongshe.com/reaction/1158139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPivaloyl chlorideHCID 62493—
ReactantLithium ChlorideHCID 433294—
Reactant(R)-4-Benzyl-2-oxazolidinoneHCID 2734969—
Reactant8-(4-Fluoro-3-methylphenyl)octanoic acidHCID 59512594—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 59512572HCID 5951257290.4%

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a cooled (−10° C.) solution of 8-(4-fluoro-3-methylphenyl)octanoic acid (0.452 g, 1.791 mmol) in 15 mL of THF, were added stepwise triethylamine (0.67 mL, 4.836 mmol) and pivaloyl chloride (0.24 mL, 1.971 mmol). The reaction mixture was stirred at −10° C. for 1 h and then LiCl (0.084 g, 1.971 mmol) and (R)-4-benzyloxazolidin-2-one (0.349 g, 1.971 mmol) were added stepwise. After warming slowly to room temperature and stirring overnight, the reaction mixture was diluted with ethyl acetate (80 mL) and washed with saturated NaHCO3 solution and brine. The organic layer was dried (Na2SO4), filtered, and concentrated under reduced pressure. The product was isolated by Flash column chromatography (silica gel column) eluting with 0-100% dichloromethane/hexanes to give the title compound as colorless oil (0.666 g, 90% yield). GC-MS: tR=9.6 min; m/z 411 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807720B2
Source datasetuspto-grants-2010_10
ORD IDord-ec8971d2c83b4fe295204f5accccb32e
Source noteuspto-grants-2010_10