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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452286Generated: October 30, 2026

Triethylamine → HCID 19972641, compound

https://huagongshe.com/reaction/1452286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantMethylamine hydrochlorideHCID 6364545—
ReactantHCID 19972556HCID 19972556—
CatalystZincchlorideHCID 3007855—
SolventMethanolHCID 887—
ProductHCID 19972641HCID 1997264178.8%

Reaction Steps

A solution of 15.1 g of anhydrous zinc chloride and 14.5 g of sodium cyanoborohydride in 400 ml of anhydrous methanol was added dropwise at 0° C. into a stirred mixture of 58.8 g of 8-formyl-3-methyl-4-oxo-2-phenyl-4H-1-benzopyran, 60.7 g of methylamine hydrochloride and 125 ml of triethylamine in 600 ml of anhydrous methanol. After stirring for 5 hours at 20°-25° C., the solvent was evaporated off in vacuo and the residue was taken up in 200 ml of water and collected by suction filtration. The crude product was dissolved in aqueous acetic acid, washed with ethyl acetate and re-precipitated by addition of cold 6N aqueous sodium hydroxide solution. 49 g of the title compound was obtained. m.p. 97°-99° C., after crystallization from 75% ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05605896
Source datasetuspto-grants-1997_02
ORD IDord-e0a91c6b64e444de8a5b45b6db1819f5
Source noteuspto-grants-1997_02