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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091135Generated: November 2, 2026

Formaldehyde → HCID 53726018, compound

https://huagongshe.com/reaction/1091135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium HydroxideHCID 14798—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 20098373HCID 20098373—
CatalystZincchlorideHCID 3007855—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 53726018HCID 5372601872.9%

Reaction Steps

Under an inert atmosphere, a solution of 0.2 g of 2[3-[[2-(3,4-dimethoxyphenyl)ethyl]amino]-2-hydroxypropoxy]-N-(1H-indol-4-yl) -benzamide in 5 ml of methanol in the presence of 0.1 ml of formaldehyde with 40% of water was admixed with a solution of 26 mg of sodium cyanoborohydride and 27.2 mg of zinc chloride in 5 ml of methanol and the reaction mixture was left for 2 hours at ambient temperature. 5 ml of 0.1N sodium hydroxide were added, and the mixture was extracted with ethyl acetate. The organic phase was washed with water, dried, and the solvents were eliminated under reduced pressure to obtain 0.230 g of crude product. It was purified by chromatography over silica (eluent: chloroform - ethyl acetate - triethylamine, 6-3-1) to obtain 0.150 g of 2-[3-[[2-(3,4-dimethoxyphenyl)ethyl]methylamino]-2-hydroxypropoxy]-N-(1H-indol-4-yl)-benzamide

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05084455
Source datasetuspto-grants-1992_01
ORD IDord-c32e45a655f94d599633257c3e757798
Source noteuspto-grants-1992_01