Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862711Generated: October 31, 2026

Sodium borohydride → HCID 178498838, compound

https://huagongshe.com/reaction/862711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 19698828HCID 19698828—
SolventEthanolHCID 702—
ProductHCID 178498838HCID 178498838122.6%

Reaction Steps

0.170 g (3 eq) of sodium borohydride is added to 0.400 g of 1-methyl-2-veratrylamino-5-methoxycarbonylpyrimidiniumhydroxide dissolved in 50 ml of ethanol. The mixture is stirred under argon at room temperature for three hours. After evaporation of the ethanol, the medium is extracted with dichloromethane and water. The organic phases are washed with a saturated sodium chloride solution and then dried over sodium sulfate. The oil resulting from evaporation of the organic phases, purified on silica gel under medium pressure (eluent: 15% MeOH/CH2 Cl2) gives 467 mg (yield: 98%) of the corresponding 1,6-dihydropyrimidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05719187
Source datasetuspto-grants-1998_02
ORD IDord-d8db8d0762a64d59a9d702c73a6d5a03
Source noteuspto-grants-1998_02