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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255716Generated: November 1, 2026

Sodium borohydride → HCID 20183353, compound

https://huagongshe.com/reaction/255716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 20183307HCID 20183307—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20183353HCID 2018335319.9%

Reaction Steps

The mixture of 5-acetyl-6-methyl-4-(4-nitrophenyl)-2-phenyl-pyrimidine (1.5 g) and sodium borohydride (170 mg) in methanol (15 ml) and tetrahydrofuran (20 ml) was stirred for 2 hours at 5°-7° C. with ice cooling. The mixture was extracted with chloroform (100 ml) and 10% aqueous hydrochloric acid (50 ml). The separated organic layer was washed successively with saturated sodium hydrogen carbonate, saturated aqueous sodium chloride, dried over magnesium sulfate and evaporated in vacuo. The residue is recrystallized from ether to give 5-(1-hydroxyethyl)-6-methyl-4-(4-nitrophenyl)-2-phenylpyrimidine (0.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04698340
Source datasetuspto-grants-1987_10
ORD IDord-927a1d60415d4433adea9e5027342977
Source noteuspto-grants-1987_10