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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722028Generated: October 30, 2026

HCID 178459277, compound → HCID 178459267, compound

https://huagongshe.com/reaction/722028

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178459277HCID 178459277—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
ProductHCID 178459267HCID 17845926781.2%

Reaction Steps

In 10 ml of methanol was dissolved 204 mg of N-tert-butoxycarbonyl-trans-4-(2-propen-1-yloxy)cyclohexylamine (the compound of Reference Example 9-11). 44 mg of 10% palladium-carbon was added thereto, and the mixture was stirred under hydrogen atmosphere at normal pressure, at room temperature for 2 days. The catalyst was removed by filtration and the solvent was removed and the residue was stirred in 2 ml of trifluoroacetic acid for 3 hours. The solvent was removed, and the residue was mixed with an aqueous 10% sodium hydroxide solution, extracted with chloroform and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure to obtain 102 mg of trans-4-(propoxy)cyclohexylamine (Reference Example 9-13 in Table 10).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138397B2
Source datasetuspto-grants-2006_11
ORD IDord-211217981b6342abb46def1aeadf43da
Source noteuspto-grants-2006_11