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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867335Generated: October 26, 2026

tert-butyl N-(2-methyl-4-oxobutan-2-yl)carbamate → Tert-butyl {3-[2-(1-hydroxycyclohexyl)phenylamino]-1,1-dimethylpropyl}carbamate

https://huagongshe.com/reaction/1867335

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl N-(2-methyl-4-oxobutan-2-yl)carbamateHCID 11788901—
Reactant1-(2-Aminophenyl)cyclohexan-1-olHCID 13554528—
SolventEthyl acetate hexaneHCID 21226206—
ProductTert-butyl {3-[2-(1-hydroxycyclohexyl)phenylamino]-1,1-dimethylpropyl}carbamateHCID 86600982—

Reaction Steps

The product is prepared analogously to intermediate product 1b starting from 1-(2-aminophenyl)cyclohexanol and tert-butyl (1,1-dimethyl-3-oxopropyl)carbamate. After column chromatography (silica gel, hexane/EtOAc 7:1) the product is obtained as a colorless oil. Yield: 2.65 g (66%); Rf=0.50 (silica gel, hexane/EtOAc 4:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632834B2
Source datasetuspto-grants-2009_12
ORD IDord-1b832b0984ef41dd9a1e0b28b320d152
Source noteuspto-grants-2009_12