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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1011659Generated: November 1, 2026

Benzaldehyde → 1R,2R-N,N'-bis(phenylMethyl)-1,2-CyclohexanediaMine

https://huagongshe.com/reaction/1011659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
Reactant1,2-Diaminocyclohexane, trans-HCID 43806—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
Product1R,2R-N,N'-bis(phenylMethyl)-1,2-CyclohexanediaMineHCID 1114095796%

Reaction Steps

Benzaldehyde (12.72 g, 120 mmol) was added dropwise over a period of 2 minutes to a solution of (R,R)-cyclohexane-1,2-diamine (6.84 g, 60 mmol) in 100 mL of anhydrous MeOH at refluxing temperature. After stirring for 30 min, the solution was allowed to cool to room temperature and NaBH3CN (4.8 g, 126 mmol) was added in portions. After the vigorous effervescence subsided down, the mixture was brought to refluxing and stirred for 20 min. The reaction was quenched by water and extracted with dichloromethane. The organic phase was dried and concentrated to give 16.95 g of crude product (yield 96%) which was used in the next step reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977372B2
Source datasetuspto-grants-2011_07
ORD IDord-412e03eb004848a6b1f56f379598f93b
Source noteuspto-grants-2011_07