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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257406Generated: October 26, 2026

Sulfuric Acid → 1-(3-n-Butoxy-2-hydroxypropyl)-5-ethyl-5-phenyl-(1H,3H,5H)-pyrimidine-2,4,6-trione

https://huagongshe.com/reaction/257406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantPhenobarbitalHCID 4763—
ReactantTriethylamineHCID 8471—
Reactant2-Propanol, 1-butoxy-3-chloro-HCID 27759—
SolventDimethylformamideHCID 6228—
Product1-(3-n-Butoxy-2-hydroxypropyl)-5-ethyl-5-phenyl-(1H,3H,5H)-pyrimidine-2,4,6-trioneHCID 1978312453.1%

Reaction Steps

A solution of phenobarbital (69.6 g, 0.3 mole) in dimethylformamide (60 ml) containing triethylamine (20.2 g, 0.2 mole) was stirred with 1-chloro-3-n-butoxy-2-propanol (33.2 g, 0.2 mole) for 6 hours at 70° C. The reaction mixture was then poured into 3% sulphuric acid (500 ml) and the precipitated product was extracted with toluene (200 ml) at 70° C. The toluene layer was separated, washed with 3% aqueous sulphuric acid (200 ml) and left overnight at 4° C. The precipitated phenobarbital was filtered off and filtrate extracted with 5% aqueous sodium carbonate (5×100 ml). The organic layer was then extracted with 1M aqueous sodium hydroxide (2×200 ml), the aqueous layers collected, washed with toluene (100 ml) and the pH was adjusted to 3 with sulphuric acid. The precipitated product was extracted with toluene (150 ml), the organic layer was separated, dried and evaporated under reduced pressure to give the title compound (38.5 g, 53%); purity by HPLC 96.5% .

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05262402
Source datasetuspto-grants-1993_11
ORD IDord-e726e6ac9f05453f95faec9db4973de4
Source noteuspto-grants-1993_11