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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259832Generated: October 30, 2026

Ammonium formate → 2(S)-amino-1-cyclohexyl-3(S)-hydroxy-6-methylheptane

https://huagongshe.com/reaction/259832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant2(S)-(N,N-Dibenzylamino)-1-cyclohexyl-3(S)-hydroxy-6-methylheptaneHCID 54304065—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
Product2(S)-amino-1-cyclohexyl-3(S)-hydroxy-6-methylheptaneHCID 14671722148.1%

Reaction Steps

2(S)-(N,N-Dibenzylamino)-1-cyclohexyl-3(S)-hydroxy-6-methylheptane (5 g) was dissolved in methanol (50 ml). Ammonium formate (6.18 g) and then 10% palladium-carbon (50% wet, 0.5 g) were added thereto, and the mixture was vigorously stirred at room temperature. After the completion of the reaction, the reaction mixture was filtered, and the filtrate was concentrated under reduced pressure. Ethyl acetate and water were added to the concentrated residue for extraction. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give 4.13 g of 2(S)-amino-1-cyclohexyl-3(S)-hydroxy-6-methylheptane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05523410
Source datasetuspto-grants-1996_06
ORD IDord-fd8dddd55e1c422eb61b0cff155d2803
Source noteuspto-grants-1996_06