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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1460619Generated: November 2, 2026

Formaldehyde → trans-3,4-dihydro-3-hydroxy-4-[N-(2-hydroxymethyl-3-oxo-cyclopent-1-enyl)amino]-2,2-dimethyl-2H-1-benzopyran-6-carbonitrile

https://huagongshe.com/reaction/1460619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantPhenolphthaleinHCID 4764—
ReactantSodium HydroxideHCID 14798—
Reactanttrans-3,4-dihydro-3-hydroxy-2,2-dimethyl-4-(3-oxo-1-cyclopent-1-enylamino)-2H-1-benzopyran-6-carbonitrileHCID 14301304—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Producttrans-3,4-dihydro-3-hydroxy-4-[N-(2-hydroxymethyl-3-oxo-cyclopent-1-enyl)amino]-2,2-dimethyl-2H-1-benzopyran-6-carbonitrileHCID 14301320—

Reaction Steps

2,98 of the title compound of example 5 are dissolved in 150 ml of acetone and a drop of a phenolphtalein-solution and the solution is mixed with 2,5 ml of a 37% formaldehyde solution three times every hour. The pH-value of the solution is kept between 8 and 9 by controlled addition of 0,1 aq. sodium hydroxide-solution. After stirring during 5 hours the reaction solution is diluted with water and the organic components are extracted with dichloromethane. Usual work up yields white crystalls of the title compound having a m.p. of 218°-220° C. (from dichloromethane/ethanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05071871
Source datasetuspto-grants-1991_12
ORD IDord-f7e23cbb60d94b99ae3b0bde73b548ee
Source noteuspto-grants-1991_12