Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414201Generated: October 29, 2026

Formaldehyde → HCID 53726018, compound

https://huagongshe.com/reaction/414201

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 numberUS04791109
Source datasetuspto-grants-1988_12
ORD IDord-10399656b5594d75bbad6188e2bcf6a2
Source noteuspto-grants-1988_12