Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171574Generated: November 1, 2026

Trifluoroacetic acid → HCID 68767536, compound

https://huagongshe.com/reaction/1171574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 68765533HCID 68765533—
SolventDichloromethaneHCID 6344—
ProductHCID 68767536HCID 6876753659%

Reaction Steps

A solution of (1R,2S,5R)-methyl 2-((S)-3-(benzyloxycarbonylamino)-2-oxopyrrolidin-1-yl)-5-(tert-butoxycarbonylamino)-cyclohexanecarboxylate in CH2Cl2 (10 mL) was treated with TFA (15 mL) and stirred at room temperature for 2 h. The reaction mixture was concentrated in vacuo and the residue dissolved in CH2Cl2 and washed with NaHCO3(aq), brine, and dried over MgSO4. The solution was filtered and concentrated in vacuo to give 0.75 g (59%) of (1R,2S,5R)-methyl 5-amino-2-((S)-3-(benzyloxycarbonylamino)-2-oxopyrrolidin-1-yl)cyclohexanecarboxylate as a white solid. MS found: (M+H)+=390.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829571B2
Source datasetuspto-grants-2010_11
ORD IDord-4d3a020220964f6ba28d8f15b8d3b43f
Source noteuspto-grants-2010_11