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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982641Generated: November 1, 2026

Dicyclohexylcarbodiimide → (S)-Phenylmethyl 2-[[1-[[[2-(1,1-dimethylethoxy)-2-oxoethyl]amino]carbonyl]-3-methylbutoxy]methyl]-1-pyrrolidinecarboxylate

https://huagongshe.com/reaction/1982641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant(2S)-phenylmethyl 2-[(1-carboxy-3-methylbutoxy)methyl]-1-pyrrolidinecarboxylateHCID 57212195—
Reactanttert-ButylglycinateHCID 77068310—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product(S)-Phenylmethyl 2-[[1-[[[2-(1,1-dimethylethoxy)-2-oxoethyl]amino]carbonyl]-3-methylbutoxy]methyl]-1-pyrrolidinecarboxylateHCID 70468867—

Reaction Conditions

Temperature0 °C

Reaction Steps

(2S)-Phenylmethyl-2-[(1-carboxy-3-methylbutoxy)methyl]-1-pyrrolidinecarboxylate (center on side chain is R,S mixture), 2 g (0.0057 mol), is dissolved in 100 ml of dichloromethane, cooled to 0° C. and 1.1 g (0.0084 mol) of t-butylglycinate, 0.88 g (0.0057 mol) of 1-hydroxybenzotriazole and 1.32 g (0.0064 mol) of dicyclohexylcarbodiimide are added. The mixture is allowed to reach room temperature and stirred 14 hours, filtered, the solvent evaporated in vacuo and the residue dissolved in 200 ml of dichloromethane and washed successively with a 5% aqueous solution of sodium chloride, 2×200 ml. The dichloromethane layer is separated, dried over sodium sulfate, evaporated in vacuo and the residue purified by chromatography using silica gel and eluting with dichloromethane-methanol (98:2) to give (S)-phenylmethyl 2-[[1-[[[2-(1,1-dimethylethoxy)-2-oxoethyl]amino]carbonyl]-3-methoxy-butoxy]methyl]-1-pyrrolidinecarboxylate (2-position of pentane chain is R S), 1.75 g; [ α]D25 -70.2° (c 0.39, methanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04596819
Source datasetuspto-grants-1986_06
ORD IDord-4f3a0b13dad54182bff78691e37f34ac
Source noteuspto-grants-1986_06