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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28428Generated: October 25, 2026

Triethylamine → (4R,5S)-4-Methyl-3-((R)-4-methyl-heptanoyl)-5-phenyl-oxazolidin-2-one

https://huagongshe.com/reaction/28428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPivaloyl chlorideHCID 62493—
ReactantLithium ChlorideHCID 433294—
Reactant(4R,5S)-(+)-4-Methyl-5-phenyl-2-oxazolidinoneHCID 2733812—
Reactant4-Methylheptanoic acid, (-)-HCID 13800370—
SolventTetrahydrofuranHCID 8028—
Product(4R,5S)-4-Methyl-3-((R)-4-methyl-heptanoyl)-5-phenyl-oxazolidin-2-oneHCID 57160957—

Reaction Steps

To (R)-4-methyl-heptanoic acid (19 g, 0.132 mol) and triethylamine (49.9 g, 0.494 mol) in THF (500 mL) at 0° C. was added trimethylacetylchloride (20 g, 0.17 mol). After 1 hour LiCl (7.1 g, 0.17 mol) was added followed by (4R,5S)-(+)-4-methyl-5-phenyl-2-oxazolidinone) 3 (30 g, 0.17 mol). The mixture was warmed to room temperature and after 16 hours the filtrate was removed by filtration and the solution concentrated under reduced pressure. Flash chromatography (7:1 hexane/EtOAc) gave (4R,5S)-4-methyl-3-((R)-4-methyl-heptanoyl)-5-phenyl-oxazolidin-2-one as an oil. 31.5 g; 79%. [a]D=+5.5 (c 1 in CHCl3). MS, m/z (relative intensity): 304 [M+H, 100%].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07419981B2
Source datasetuspto-grants-2008_09
ORD IDord-618a4a3542234e029cb50fd22681dc1f
Source noteuspto-grants-2008_09