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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733309Generated: October 31, 2026

3-n-Butyl-5-(2,4,5-trimethoxybenzylidene) hydantoin → 3-n-Butyl-5-(2,4,5-trimethoxybenzyl) hydantoin

https://huagongshe.com/reaction/1733309

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-n-Butyl-5-(2,4,5-trimethoxybenzylidene) hydantoinHCID 53964282—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
Product3-n-Butyl-5-(2,4,5-trimethoxybenzyl) hydantoinHCID 12790722—

Reaction Steps

3-n-Butyl-5-(2,4,5-trimethoxybenzylidene) hydantoin (10.0 g; 0.03 mole) was mixed with glacial acetic acid (150 ml.) and hydrogenated in a Parr apparatus in the presence of 5% Pd/C (2 g). After 2 hours the catalyst was filtered off, washed with warm acetic acid and the colourless filtrate evaporated in vacuo to give a white crystalline solid. Recrystallisation from ethyl acetate gave the title compound, yield 9.2 g (91%), m.p. 122° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04241073
Source datasetuspto-grants-1980_12
ORD IDord-6f04df223d1041bb9710dedd9f003c9e
Source noteuspto-grants-1980_12