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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867600Generated: October 27, 2026

Dicyclohexylcarbodiimide → BOC-Ala-Gly-OBzl

https://huagongshe.com/reaction/867600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantN-HydroxysuccinimideHCID 80170—
ReactantTert-butoxycarbonylalanineHCID 85082—
ReactantO-benzylglycine toluene-p-sulphonateHCID 6451311—
SolventAcetonitrileHCID 6342—
SolventTriethylamineHCID 8471—
ProductBOC-Ala-Gly-OBzlHCID 10980600—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 12.9 g of glycine benzyl ester tosylate in 200 ml acetonitrile cooled to 0° C., was added dropwise triethylamine (5.3 ml), followed by addition of 12 g of N-tert-butyloxycarbonylalanine N-hydroxysuccinimide ester (prepared by reaction of N-tert-butyloxycarbonylalanine with N-hydroxysuccinimide in the presence of dicyclohexylcarbodiimide). The resulting solution was stirred at 0° C. for one hour and then at room temperature for 18 hours. At the end of reaction, the solvent was distilled off under reduced pressure, the residue was extracted with ethyl acetate, and the extract was washed with 5% acetic acid, water and saturated aqueous solution of sodium chloride in that order, giving 16 g of crude product. Purification of this crude product by silica gel chromatography (chloroform:methanol=40:1) afforded 12.6 g of pure N-tert-butyloxycarbonyl-L-alanyl-glycine benzyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04775743
Source datasetuspto-grants-1988_10
ORD IDord-0d6270590ae0427e81ba43fb2895bb4b
Source noteuspto-grants-1988_10