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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377798Generated: October 31, 2026

Acetic Acid → {4-[4-(2-Isopropoxy-phenyl)-piperidin-1-yl]-cyclohexyl}-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/2377798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactanttert-butyl N-(4-oxocyclohexyl)carbamateHCID 1512535—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-(2-Isopropoxyphenyl)piperidineHCID 10536874—
SolventDichloromethaneHCID 6344—
Product{4-[4-(2-Isopropoxy-phenyl)-piperidin-1-yl]-cyclohexyl}-carbamic acid tert-butyl esterHCID 5871270648%

Reaction Steps

A (4-oxo-cyclohexyl)-carbamic acid tert-butyl ester Compound 1b (1.54 g, 7.21 mmol), NaBH(OAc)3 (64.45 g, 21.0 mmol) and HOAc (0.3 mL) were added to a solution of 4-(2-isopropoxy-phenyl)-piperidine Compound 1a (1.32 g, 6.01 mmol) in CH2Cl2 (100 mL). The mixture was stirred under N2 for two days, then the reaction was quenched with MeOH. The mixture was evaporated and the resulting residue was redissolved with CH2Cl2, washed using 10% aqueous Na2CO3 and brine, then dried (Na2SO4). The crude product was purified by column chromatography to provide {4-[4-(2-isopropoxy-phenyl)-piperidin-1-yl]-cyclohexyl}-carbamic acid tert-butyl ester Compound 1c as a mixture of cis/trans isomers (MS 416; yellowish oil; 1.19 g, 48% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470711B2
Source datasetuspto-grants-2008_12
ORD IDord-ae5e799bd3b544039e270fad6db9d4dd
Source noteuspto-grants-2008_12