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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888352Generated: October 29, 2026

1,2-Dichloroethane → Tert-butyl (R)-(1-(3-methyl-1,2,4-oxadiazol-5-YL)ethyl)carbamate

https://huagongshe.com/reaction/888352

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantEthyl AcetateHCID 8857—
ReactantN-HydroxyacetamidineHCID 30926—
ReactantBOC-D-alanineHCID 637606—
SolventDimethylformamideHCID 6228—
Solvent1,4-DioxaneHCID 31275—
ProductTert-butyl (R)-(1-(3-methyl-1,2,4-oxadiazol-5-YL)ethyl)carbamateHCID 8665702524.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of N-(tert-butoxycarbonyl)-D-alanine (20 g, 106 mmol), acetamide oxime (17.3 g, 234 mmol) in 120 mL of 1,4-dioxane and 30 mL of N,N-dimethylformamide were added EDC (44.8 g, 234 mmol). The mixture was heated at 60° C. for 4 h then at 100° C. for 16 h. After cooling to ambient temperature, 300 mL of ethyl acetate was added. The mixture was washed with aqueous saturated sodium bicarbonate (2×). The combined organic extracts were dried over magnesium sulfate, filtered and concentrated. The residue was purified by silica gel chromatography (100% dichloromethane→90% dichloromethane/methanol) to give pure tert-butyl[(1R)-1-(3-methyl-1,2,4-oxadiazol-5-yl)ethyl]carbamate (6.0 g). MS 172.1 ((M-t-butyl+H)+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247401B2
Source datasetuspto-grants-2012_08
ORD IDord-318238a87a6b471da44c0b091655dcd5
Source noteuspto-grants-2012_08