Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743834Generated: November 1, 2026

Sodium cyanoborohydride → HCID 10466921, compound

https://huagongshe.com/reaction/1743834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 10354280HCID 10354280—
SolventAcetic AcidHCID 176—
ProductHCID 10466921HCID 1046692161.9%

Reaction Steps

To a solution 2,3,4,5,9,10,11,12-octahydro-1H-[1,4]diazocino[7,8,1-jk]carbazole (0.20 g, 0.80 mmole) in acetic acid (50 mL) was added sodium cyanoborohydride (0.30 g, 4.5 mmol) and the reaction mixture was stirred at room temperature for 1 hour. The solvent was removed in vacuo and the residue was diluted with ethyl acetate (300 mL) and washed with saturated aqueous sodium bicarbonate (150 mL) and saturated aqueous sodium chloride (150 mL), dried (sodium sulfate) and concentrated in vacuo. Purification by flash column chromatography (silica gel, ethyl acetate:hexanes 3:2) provided 0.12 g of the title compound as an oil. This compound was treated with one equivalent of fumaric acid in ethanol to form a fumarate salt, mp 169-171° C. MS (ESI) m/z 243 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07012089B2
Source datasetuspto-grants-2006_03
ORD IDord-69b598f0e18b4dcabebec904929852a2
Source noteuspto-grants-2006_03