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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642489Generated: October 31, 2026

1,2-Diaminocyclohexane, cis- → HCID 66757269, compound

https://huagongshe.com/reaction/1642489

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-Diaminocyclohexane, cis-HCID 342917—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 10990126HCID 10990126—
SolventDichloromethaneHCID 6344—
ProductHCID 66757269HCID 66757269—

Reaction Steps

To a solution of cis-cyclohexane-1,2-diamine (0.850 mL, 7.22 mmol) in dichloromethane (10 mL) was added with tert-butyl 4-methyl-4-(4-oxo-1-piperidyl)piperidine-1-carboxylate (1.39 g, 3.61 mmol) in dichloromethane (5 mL) followed by sodium triacetoxyborohydride (0.918 g, 4.33 mmol) and the mixture stirred at room temperature over night. The mixture was then quenched with 1 N NaOH and dichloromethane was added. The phases were separated and aqueous phase was extracted with dichloromethane. The combined organic phases were dried and concentrated in vacuo to give the title product, which was used for the subsequent step without further purification. MS (M+1): 395.37.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119661B2
Source datasetuspto-grants-2012_02
ORD IDord-9683303a190b424db3f802e4c9a8a5b2
Source noteuspto-grants-2012_02