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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227261Generated: October 29, 2026

Triethylamine → HCID 11437716, compound

https://huagongshe.com/reaction/2227261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Acetylbutyric acidHCID 18407—
ReactantPivaloyl chlorideHCID 62493—
Reactant(S)-4-Benzyl-2-oxazolidinoneHCID 736225—
ReactantLithiumHCID 3028194—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 11437716HCID 11437716—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 4-acetylbutyric acid 1-7 (25.0 g, 192 mmol), triethylamine (29.5 ml, 211 mmol) in tetrahydrofuran (500 mL) at −78° C. was added pivaloyl chloride (26.0 ml, 211 mmol). After 20 min, the mixture was warmed to 0° C. for 1.0 h and then recooled to −78° C. To a stirred solution of (S)-(−)-4-benzyl-2-oxazolidinone (37.4 g, 211 mmol) in tetrahydrofuran (500 ml) at −78° C. was added nBuLi (84.5 ml, 211 mmol, 2.5M in hexanes) dropwise over 10 minutes. After 20 minutes, the lithium reagent was transferred to the mixed anhydride via cannula. After 10 minutes, the reaction was warmed to 0° C. for 1.0 h. The mixture was diluted with ethyl acetate, washed with saturated aqueous sodium hydrogen carbonate, saturated aqueous sodium chloride, and dried over anhydrous magnesium sulfate. The reaction mixture was filtered and concentrated at reduced pressure to give 1-8 as a solid which was triturated with ethyl ether and filtered to give a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06413955B1
Source datasetuspto-grants-2002_07
ORD IDord-a32f826d55b445fd9b9c5ee8c7c91e45
Source noteuspto-grants-2002_07