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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65712Generated: October 29, 2026

1-(2-ethoxycarbonylpropanoyl)-L-proline tert.-butyl ester → 1-(2-ethoxycarbonylpropanoyl)-L-proline

https://huagongshe.com/reaction/65712

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-ethoxycarbonylpropanoyl)-L-proline tert.-butyl esterHCID 70610337—
SolventTrifluoroacetic acidHCID 6422—
Product1-(2-ethoxycarbonylpropanoyl)-L-prolineHCID 53678547—

Reaction Steps

The ester obtained in Example 2 (5.9 g.) is dissolved in trifluoroacetic acid, the solution is kept at room temperature for one hour, and then concentrated to dryness in vacuo. The residue is dissolved in a mixture of ethyl acetate and saturated aqueous sodium bicarbonate. The aqueous phase is acidified and extracted with ethyl acetate. The ethyl acetate layer is dried over magnesium sulfate and concentrated to dryness in vacuo to obtain 1-(2-ethoxycarbonylpropanoyl)-L-proline, yield 4.1 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04128653
Source datasetuspto-grants-1978_12
ORD IDord-7f533fadaa4d4ac68b417529015fe1cd
Source noteuspto-grants-1978_12