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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1450141Generated: October 26, 2026

Phenobarbital → 5-Ethyl-6-hydroxy-3-(4-methoxycarbonylbutyl)-5-phenyl-2,4(3H,5H)-pyrimidinedione

https://huagongshe.com/reaction/1450141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenobarbitalHCID 4763—
ReactantSodium ChlorideHCID 5234—
ReactantMethyl 5-bromovalerateHCID 79557—
ReactantTetrabutylammonium HydroxideHCID 2723671—
SolventDichloromethaneHCID 6344—
Product5-Ethyl-6-hydroxy-3-(4-methoxycarbonylbutyl)-5-phenyl-2,4(3H,5H)-pyrimidinedioneHCID 178435245—

Reaction Steps

A mixture of phenobarbital (46.5 g, 0.2 mole) and tetrabutylammonium hydroxide (500 mL, 0.2 mole of 0.4M in water) in dichloromethane (500 mL) was prepared and to it was added methyl 5-bromovalerate (39.0 g, 0.2 mole). The reaction mixture was stirred vigorously overnight (20 hrs). To this mixture was added saturated sodium chloride solution (100 mL), the organic layer was separated, and the aqueous solution was washed with dichloromethane (2×100 mL). The combined organic solution was washed with saturated sodium chloride solution (100 mL), dried over anhydrous MgSO4, filtered, and the solvent removed.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05601994
Source datasetuspto-grants-1997_02
ORD IDord-8952355646a94cbca3eb341036e71988
Source noteuspto-grants-1997_02