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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380121Generated: October 28, 2026

Ammonium Chloride → HCID 14989076, compound

https://huagongshe.com/reaction/2380121

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant(4S)-4-(propan-2-yl)-1,3-oxazolidin-2-oneHCID 7157133—
Reactant3-(4-Methoxyphenyl)propionyl chlorideHCID 10932441—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 14989076HCID 1498907680%

Reaction Steps

18.19 ml (29.1 mmoles) of butyllithium (as a 1.6M hexane solution) were added dropwise at -78° C. and under an atmosphere of nitrogen to a solution of 3.13 g (24.2 mmoles) of 4(S)-isopropyl-2-oxazolidinone in 50 ml of anhydrous tetrahydrofuran, and then the mixture was stirred for 30 minutes. At the end of this time, a solution of 5.43 g (29.1 mmoles) of 3-(4-methoxyphenyl)propionyl chloride in 20 ml of anhydrous tetrahydrofuran was added dropwise to the resulting mixture over the course of 10 minutes. The mixture was then stirred for a further 1 hour, after which a saturated aqueous solution of ammonium chloride was added to the reaction mixture, which was then extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate, and the solvent was removed by distillation under reduced pressure. The resulting residue was purified by medium pressure silica gel column chromatography (using a 1:3 by volume mixture of ethyl acetate and hexane as eluent), followed by recrystallization from diisopropyl ether, to give 5.63 g (yield 80%) of the title compound as white crystals, melting at 62.0°-63.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05364844
Source datasetuspto-grants-1994_11
ORD IDord-2fff1a43e5684c94867ca1a878bb732d
Source noteuspto-grants-1994_11