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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894102Generated: October 30, 2026

Cyclopentanone → HCID 53687650, compound

https://huagongshe.com/reaction/894102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentanoneHCID 8452—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 2736334HCID 2736334—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 53687650HCID 53687650—

Reaction Steps

A solution of p-glycidyloxybenzaldehyde (40 g; prepared according to Method A) and cyclopentanone (9.4 g) in ethanol (40 g) was added over 1 hour to a stirred solution of sodium hydroxide (2.25 g) in a mixture of water (45 g) and ethanol (40 g), keeping the temperature at 25° to 30° C. On complete addition the mixture was stirred at 25° to 30° C. for a further 30 minutes, then water (100 g) was added and the mixture was stirred for 15 minutes. The precipitate was filtered off, washed with water and ice-cold ethanol, and dried at 60° C. in vacuo to give 1,3-bis(p-glycidyloxyphenylmethylidene)cyclopentan-2-one. The yield was 40 g (88% of theory) and the product had an epoxide content of 4.43 equivalents per kilogram, the theoretical value being 4.95 equivalents per kilogram. The N.M.R., I.R., and UV spectra of the product were consistent with the above structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04282353
Source datasetuspto-grants-1981_08
ORD IDord-571992d467c5472482e41e089b4a2d10
Source noteuspto-grants-1981_08