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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374431Generated: October 30, 2026

Sodium borohydride → HCID 178498838, compound

https://huagongshe.com/reaction/374431

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-methoxycarbonylpyrimidinium hydroxide 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/CH2Cl2) gives 467 mg (yield: 98%) of the corresponding 1,6-dihydropyrimidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05480884
Source datasetuspto-grants-1996_01
ORD IDord-442fd9acca7948e98d873fc98cd9997a
Source noteuspto-grants-1996_01