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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796151Generated: October 30, 2026

Ethyl Acetate → (E)-(R)-2-((S)-1-Hydroxy-2-morpholin-4-yl-2-oxo-ethyl)-5-phenyl-pent-4-enoic acid methyl ester

https://huagongshe.com/reaction/1796151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantBromomethylstyreneHCID 98116—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant(S)-3-Hydroxy-4-morpholin-4-yl-4-oxo-butyric acid methyl esterHCID 58619497—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product(E)-(R)-2-((S)-1-Hydroxy-2-morpholin-4-yl-2-oxo-ethyl)-5-phenyl-pent-4-enoic acid methyl esterHCID 6943738450%

Reaction Steps

Lithium hexamethyldisilazide (1M in THF, 14.5 ml, 14.5 mmol) was added to a solution of (S)-3-Hydroxy-4-morpholin-4-yl-4-oxo-butyric acid methyl ester (1.5 g, 6.9 mmol) in dry THF (15 ml) at −78° C. under N2 and stirred for 30 min. Cinnamyl bromide (1.6 g, 7.32 mmol) was then added, the reaction mixture stirred at −78° C. for 2 hrs, warmed up to room temperature and stirred overnight at room temperature. The reaction was quenched with saturated ammonium chloride solution, adjusted the pH to 6 with 1N HCl and extracted with ethyl acetate. Combined ethyl acetate extracts were dried over MgSO4 and concentrated under reduced pressure to give yellow solid. Column chromatography on silica eluting with a mixture of ethyl acetate and methylene chloride gave the title compound as pale yellow solid (1.15 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07030116B2
Source datasetuspto-grants-2006_04
ORD IDord-c760e8a45e844358bcd08023211adf67
Source noteuspto-grants-2006_04