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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 967143Generated: November 3, 2026

HCID 178484035, compound → HCID 178484032, compound

https://huagongshe.com/reaction/967143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178484035HCID 178484035—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178484032HCID 17848403295%

Reaction Steps

0.62 g (2.03 mmol) trans-[4-(2-hydroxy-ethyl)-cyclohexylmethyl]-methyl-carbamic acid benzyl ester dissolved in 10 ml of tetrahydrofuran were submitted to a hydrogenation over 0.3 g of 5% palladium on charcoal as catalyst, at normal pressure and ambient temperature. The cleavage of the benzyloxycarbonyl group was complete after 3 hours. After removal of the catalyst by filtration and evaporation of the solvent, 0.33 g (95%) of trans-2-(4-methylaminomethyl-cyclohexyl)-ethanol were obtained as a colorless oil, MS: 172 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06953806B2
Source datasetuspto-grants-2005_10
ORD IDord-88df80d51213460c965ce9f4bfd786ce
Source noteuspto-grants-2005_10