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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374191Generated: October 31, 2026

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

https://huagongshe.com/reaction/1374191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantPivaloyl chlorideHCID 62493—
Reactant2-OxazolidinoneHCID 73949—
ReactantLithium ChlorideHCID 433294—
Reactant4-Methylheptanoic acid, (-)-HCID 13800370—
Product(4R,5S)-4-Methyl-3-((R)-4-methyl-heptanoyl)-5-phenyl-oxazolidin-2-oneHCID 57160957—

Reaction Steps

To the acid 99 (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 the oxazolidinone (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 the product 100 as an oil. 31.5 g; 79%. [α]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 numberUS07164034B2
Source datasetuspto-grants-2007_01
ORD IDord-c8837462451d4de48b0f635c6f5e5b42
Source noteuspto-grants-2007_01