Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596212Generated: November 1, 2026

Triethylamine → 1,2-Pyrrolidinedicarboxylic acid, 1-(1,1-dimethylethyl) ester, (2S)-

https://huagongshe.com/reaction/596212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,4-DioxaneHCID 31275—
Reactant2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrileHCID 93865—
ReactantL-ProlineHCID 145742—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product1,2-Pyrrolidinedicarboxylic acid, 1-(1,1-dimethylethyl) ester, (2S)-HCID 8508378.6%

Reaction Steps

2-tert-Butoxycarbonyloxyimino-2-phenylacetonitrile (1.25 g.) was added to a solution of L-proline (575 mg.) and triethylamine (0.7 ml.) in a mixture of methanol (7.5 ml.), dioxane (2.5 ml.) and water (5.0 ml.) at room temperature, and the mixture was stirred for 1.5 hours at room temperature. The reaction mixture was concentrated under reduced pressure, and to the residue were added benzene and water. After shaking the resultant mixture, the aqueous layer was separated from the mixture, washed with benzene, acidified with hydrochloric acid, and extracted with ethyl acetate. The extract was washed with water, dried over magnesium sulfate and concentrated. To the residue was added a mixture of ether and n-hexane and the precipitated crystals were collected by filtraton and dried to give N-tert-butoxycarbonyl-L-proline (845 mg.), mp 133° to 134° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04010178
Source datasetuspto-grants-1977_03
ORD IDord-e0c1d05d6b5f47108291469652412eb2
Source noteuspto-grants-1977_03