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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25563Generated: October 29, 2026

Water → HCID 178485998, compound

https://huagongshe.com/reaction/25563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 178486000HCID 178486000—
SolventTetrahydrofuranHCID 8028—
Product1-Aminocyclohexan-1-olHCID 14739837—
ProductHCID 178485998HCID 178485998180.4%

Reaction Steps

To a solution of 3.1 g (8 mmol) trans-[4-(tert-Butyl-dimethyl-silanyloxy)-cyclohexyl]-methyl-carbamic acid benzyl ester in 20 ml THF, 10.3 ml (1M, 10.3 mmol, 1.3 eq) Tetrabutylammonium fluoride in THF were added at 6° C. and the mixture was stirred at RT for 2 days. Water was added and the phases were separated and the inorganic phase was extracted with ether and EtOAc. The combined organic phases were washed with brine, dried over Na2SO4 and evaporated. Column chromatography on silica gel with a gradient EtOAc:hexane 1:4-EtOAc yielded 1.9 g 1.9 g (92%) trans-(4-Hydroxy-cyclohexyl)-methyl-carbamic acid benzyl ester as orange oil, MS: 263 (M).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858651B2
Source datasetuspto-grants-2005_02
ORD IDord-f22eaee395a747fdac90cb59abf0b2f3
Source noteuspto-grants-2005_02