Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633330Generated: November 3, 2026

Sodium borohydride → HCID 12508669, compound

https://huagongshe.com/reaction/1633330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 12508656HCID 12508656—
CatalystSodium HydroxideHCID 14798—
SolventEthanolHCID 702—
ProductHCID 12508669HCID 1250866990.3%

Reaction Steps

To a mixture of 70 grams of 5-methyl-2,6,8,9-tetraethyl-1,3,7-triazabicyclo (3,3,1) non-3-ene, 0.5 grams of sodium hydroxide, and 190 grams of ethanol was added, with stirring, over a 1/2 hour period 9 grams of sodium borohydride. The mixture was stirred for 20 hours at ambient temperature. The ethanol was removed under diminished pressure and the resulting product was added to water and extracted with ether. The ethereal solution, after drying over anh. MgSO4, was evaporated under diminished pressure to yield 64.2 grams of 5-(2-azapentyl)-5-methyl-2,4,6-triethylhexahydropyrimidine, b.p. 138°-150° C./20 torr.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04480095
Source datasetuspto-grants-1984_10
ORD IDord-5641177489ca4d79bf9681b34f631b0a
Source noteuspto-grants-1984_10