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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1984933Generated: November 3, 2026

HCID 178453922, compound → HCID 178511524, compound

https://huagongshe.com/reaction/1984933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178453922HCID 178453922—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 178511524HCID 17851152491%

Reaction Steps

A solution of cis-[4-(2-benzyloxycarbonylamino-ethyl)-cyclohexyl]-carbamic acid tert-butyl ester (5.26 g, 14 mmol) in 50% TFA in CH2Cl2 (60 mL) was stirred at ambient temperature for 1 hr. The mixture was concentrated and the residue was diluted with saturated aqueous NaHCO3. The aqueous layer was extracted with CH2Cl2 (therr times). The organic layer was dried over Na2SO4 and concentrated to give cis-[2-(4-amino-cyclohexyl)-ethyl]-carbamic acid benzyl ester (3.5 g, 91%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544690B2
Source datasetuspto-grants-2009_06
ORD IDord-466a9ac5b15140f08d499d89d4397345
Source noteuspto-grants-2009_06