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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179039Generated: October 30, 2026

Sodium Hydroxide → HCID 69338491, compound

https://huagongshe.com/reaction/1179039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantMethylamine hydrochlorideHCID 6364545—
Reactant4-Benzyl-4-(dimethylamino)cyclohexanoneHCID 20453478—
SolventAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductHCID 69338491HCID 6933849141.7%

Reaction Steps

15.0 g 4-benzyl-4-dimethylamino-cyclohexanone (see example 3) were dissolved in 225 ml analytical grade tetrahydrofuran, and 4.38 g methylamine hydrochloride, 8.9 ml triethylamine and 8.40 ml glacial acetic acid were added, while stirring in an ice-bath. 19.2 g sodium triacetoxyborohydride were then added in portions in the course of 15 minutes and the mixture was subsequently stirred overnight. For working up, 110 ml two molar sodium hydroxide solution were added dropwise (pH>10) and the mixture was extracted three times with 200 ml diethyl ether each time. The combined organic phases were washed twice with 200 ml water each time, dried over sodium sulfate and filtered and the filtrate was concentrated. The crude product obtained (15.0 g) was chromatographed over silica gel with methanol with the addition of one percent by volume of aqueous ammonia solution (25 wt. %). 11.6 g of the still significantly contaminated product were obtained, and were chromatographed again over silica gel with ethyl acetate and an addition of methanol rising from twenty-five to fifty percent by volume. 6.67 g 1-benzyl-N,N,N′-trimethyl-cyclohexane-1,4-diamine were obtained as a cis/trans mixture.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07276518B2
Source datasetuspto-grants-2007_10
ORD IDord-15e00fb37cef455a9001187c1f30c07f
Source noteuspto-grants-2007_10