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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747748Generated: October 30, 2026

Triethylamine → benzyl (3R)-3-(4-cyanobenzoylamino)-4-(3-cyanophenoxy)butanoate

https://huagongshe.com/reaction/747748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
Reactant4-Cyanobenzoyl chlorideHCID 80172—
Reactantbenzyl (3R)-3-t-butoxycarbonylamino-4-(3-cyanophenoxy)butyrateHCID 10960575—
SolventHydrochloric AcidHCID 313—
Solvent1,4-DioxaneHCID 31275—
Productbenzyl (3R)-3-(4-cyanobenzoylamino)-4-(3-cyanophenoxy)butanoateHCID 11761964—

Reaction Conditions

Temperature0 °C

Reaction Steps

1.8 g (4.38 mmol) of benzyl (3R)-3-t-butoxycarbonylamino-4-(3-cyanophenoxy)butanoate was dissolved in 20 ml of 4 N solution of hydrogen chloride in dioxane, and the solution was stirred at 0° C. for 6 hours. The solvent was evaporated, and the obtained oily residue was dissolved in 5 ml of dichloromethane. 1.09 g (6.58 mmol) of 4-cyanobenzoyl chloride and 1.22 ml (8.76 mmol) of triethylamine were added to the solution under cooling with ice, and they were stirred at room temperature overnight. The reaction mixture was treated with ethyl acetate as the extractant in an ordinary manner to obtain the crude product. After the silica gel column chromatography, the title compound was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07396844B1
Source datasetuspto-grants-2008_07
ORD IDord-acf173b28bb543d1902de9ea09a112c9
Source noteuspto-grants-2008_07