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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951910Generated: November 3, 2026

Dicyclohexylcarbodiimide → HCID 58542422, compound

https://huagongshe.com/reaction/1951910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-{[(Benzyloxy)carbonyl]amino}cyclopropane-1-carboxylic acidHCID 3589012—
Reactant(S)-methyl 2-(benzylamino)propanoateHCID 10535780—
SolventDichloromethaneHCID 6344—
ProductHCID 58542422HCID 5854242271.2%

Reaction Steps

N,N′-dicyclohexylcarbodiimide (6.0 g, 29.0 mmol) was added to a dichloromethane (150 ml) solution of methyl N-benzyl-L-alaninate (5.20 g, 26.9 mmol) and 1-{[(benzyloxy)carbonyl]amino}cyclopropanecarboxylic acid (6.30 g, 26.7 mmol) under ice cooling and the resulting mixture was stirred overnight at room temperature. The reaction mixture was concentrated under reduced pressure and then diluted with ethyl acetate, insoluble matter was removed by filtration and then the filtrate was washed with 1 N aqueous hydrochloric acid solution and saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the obtained residue was purified by silica gel column chromatography [n-hexane:ethyl acetate=1:3 (v/v)] to give the title compound (7.80 g, 71%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404691B2
Source datasetuspto-grants-2013_03
ORD IDord-a20576f1588845bb921f80a3459610b8
Source noteuspto-grants-2013_03