Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375691Generated: October 27, 2026

Tetrahydrofuran → HCID 86595499, compound

https://huagongshe.com/reaction/1375691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantCaptoprilHCID 44093—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant2-(Chloromethyl)benzoic acidHCID 296106—
ProductHCID 86595499HCID 86595499—

Reaction Steps

α-chloro-toluic acid (9.0 g, 0.0528 Mol) and carbonyldiimidazole (10.3 g, 0.0634 Mol) were dissolved in THF (100 ml) and stirred overnight at room temperature. Then TEA was added (7.4 ml. 0.0528 Mol) and to this reaction mixture a solution of captopril (11.5 g, 0.0528 Mol) in THF (20 ml) was added dropwise and the reaction was stirred overnight at room temperature. The mixture was then partitioned between KHSO4 10% and EtOAc (120 ml). The organic layer was separated and the aqueous phase was extracted with EtOAc (2×60 ml). The combined organic phases were washed with water (3×60 ml), dried over sodium sulphate and evaporated under reduced pressure affording 14.1 g of 1-[(2S)-3-(4-chloromethylbenzoyl)mercapto-2-methyl-1-oxopropyl]-L-proline as a white solid used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169805B2
Source datasetuspto-grants-2007_01
ORD IDord-6beb17abe6324a9e9032ae71c631e4f8
Source noteuspto-grants-2007_01