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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455383Generated: November 4, 2026

Trifluoroacetic acid → benzyl (S)-1-[(1S,2R,4R)-4-amino-2-propylcyclohexyl]-2-oxopyrrolidin-3-ylcarbamate

https://huagongshe.com/reaction/1455383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 68767765HCID 68767765—
SolventDichloromethaneHCID 6344—
Productbenzyl (S)-1-[(1S,2R,4R)-4-amino-2-propylcyclohexyl]-2-oxopyrrolidin-3-ylcarbamateHCID 86596857—

Reaction Steps

To a solution of {(3S)-1-[(1S,2R,4R)-4-tert-butoxycarbonylamino-2-propyl-cyclohexyl]-2-oxo-pyrrolidin-3-yl}-carbamic acid benzyl ester (3.88 g, 8.2 mmol) in CH2Cl2 (90 mL) was added TFA (45 mL) at RT. The reaction was stirred for 5 h and concentrated in vacuo. The residue was partitioned between 1N NaOH (100 mL) and EtOAc (150 mL). The aqueous layer was extracted with EtOAc (2×50 mL) and the organic phases were combined, washed with brine (25 mL), dried (Na2SO4), filtered, and concentrated in vacuo to give benzyl (S)-1-[(1S,2R,4R)-4-amino-2-propylcyclohexyl]-2-oxopyrrolidin-3-ylcarbamate. MS found: (M+H)+=374.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482335B2
Source datasetuspto-grants-2009_01
ORD IDord-df00a187e0a24f97a3dd590837f5903e
Source noteuspto-grants-2009_01