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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1922Generated: October 26, 2026

1,2-Dichloroethane → N-(t-Butoxycarbonyl)-O-Benzyl-D-Serine Allyl Ester

https://huagongshe.com/reaction/1922

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantAllyl AlcoholHCID 7858—
ReactantEthyl AcetateHCID 8857—
Reactant(R)-3-(benzyloxy)-2-((tert-butoxycarbonyl)amino)propanoic acidHCID 2733693—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductN-(t-Butoxycarbonyl)-O-Benzyl-D-Serine Allyl EsterHCID 53793486—

Reaction Steps

N-(t-Butoxycarbonyl)-O-benzyl-D-serine (600 mg; 2.03 mmol) was dissolved in dry methylene chloride (5 ml), allyl alcohol (152 μl; 2.23 mmol) and DMAP (25 mg; 0.20 mmol) added and finally EDC (428.5 mg; 2.24 mmol) added to the acid. The reaction mixture was stirred at room temperature for 2.5 h and the resulting homogeneous solution quenched with water and extracted with methylene chloride. The methylene chloride layer was washed with 5% aqueous citric acid then 10% aqueous sodium carbonate solution. The methylene chloride layer was dried over anhydrous magnesium sulfate powder, filtered and evaporated under reduced pressure to give an oil. Chromatography of the oil using ethyl acetate and hexanes 1:2 v/v afforded the product (408 mg; 60%) as a pale yellow gum. FAB-MS:- Calculated for C36H33N5 335.1; found 336.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05726319
Source datasetuspto-grants-1998_03
ORD IDord-36f08b8e5c0c4222ab2cf761a8e66449
Source noteuspto-grants-1998_03