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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704504Generated: October 31, 2026

Sodium borohydride → HCID 178432391, compound

https://huagongshe.com/reaction/704504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 178498583HCID 178498583—
SolventEthanolHCID 702—
ProductHCID 178432391HCID 178432391100.1%

Reaction Steps

In 4 liters of ethanol was suspended 45.4 g of 7-hydroxy-5-methoxycarbonyl-2-methyl-s-triazolo[1,5-a]pyrimidine and 37.83 g of sodium borohydride was added little by little thereto, and the mixture was then stirred at room temperature for 3 hours. A residue obtained by removing ethanol was dissolved in 2 liters of water, and 500 ml of Amberlite IRC-50 (H+) (trade name) was added thereto and stirred. Subsequently, the mixture was filtered and after removing water from the filtrate, 500 ml of methanol was added to the filtrate and the mixture was stirred. Then, methanol was removed from the mixture to obtain a residue. These procedures were repeated three times. Then, 500 ml of ethanol was added to the residue and the mixture was condensed. Precipitated crystals were collected by filtration, washed with ethanol and dried to obtain 39.35 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04987129
Source datasetuspto-grants-1991_01
ORD IDord-002a79495d904541806c36115d14ea69
Source noteuspto-grants-1991_01