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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399853Generated: October 27, 2026

Hydrochloric Acid → N-[1(S)-benzyl-3-hydroxy-2-oxopropyl]phthalimide

https://huagongshe.com/reaction/2399853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium ChlorideHCID 5234—
Reactant(Vinyl-2-ylidenetris(oxy))tris(trimethylsilane)HCID 553067—
Reactant3-phenyl-2(S)-phthalimidopropionyl chlorideHCID 10567197—
Solvent1,4-DioxaneHCID 31275—
ProductN-[1(S)-benzyl-3-hydroxy-2-oxopropyl]phthalimideHCID 1026731978%

Reaction Conditions

Temperature95 °C

Reaction Steps

A mixture of 134 g of 3-phenyl-2(S)-phthalimidopropionyl chloride and 269.7 g of tris(trimethylsilyloxy)ethylene was stirred at 95° C. for 5 hours. A further 54 g of tris(trimethylsilyloxy)ethylene were added and the mixture was stirred at 95° C. for a further 1.5 hours. The cooled reaction mixture was then treated with 435 ml of dioxan and 174 ml of 0.6N hydrochloric acid and the resulting mixture was heated to 85° C. for 30 minutes. The cooled mixture was saturated with sodium chloride and then extracted with diethyl ether. The ethereal solution was washed with aqueous sodium bicarbonate solution and evaporated. The resulting pale yellow solid was crystallized from ethyl acetate/n-hexane to give 103 g of N-[1(S)-benzyl-3-hydroxy-2-oxopropyl]phthalimide as a white solid, MS: m/e 310 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05451678
Source datasetuspto-grants-1995_09
ORD IDord-b0015c2e66c24ee19223a95f4c5db4be
Source noteuspto-grants-1995_09