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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164703Generated: November 1, 2026

Sodium borohydride → HCID 13088604, compound

https://huagongshe.com/reaction/2164703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 13088594HCID 13088594—
SolventIsopropanolHCID 3776—
ProductHCID 13088604HCID 1308860477.9%

Reaction Steps

9.5 g (25 millimols) of 4,4-dimethyl-1-(4-fluorophenyl)-1-phenylthio-2-(1,2,4-triazol-1-yl)-pentan-3-one (Example 3) were suspended in 150 ml of isopropyl alcohol and 0.5 g (12.5 millimols) of sodium borohydride were added in portions. After 2 days, the mixture was evaporated down in vacuo and the residue was decomposed with dilute acetic acid. The organic phase was taken up in methylene chloride, and the methylene chloride solution was washed with water, dried over sodium sulphate, filtered and evaporated down in vacuo. The crystalline residue was stirred with diisopropyl ether; the crystals were filtered off and dried. 7.5 g (77.9% of theory) of 4,4-dimethyl-1-(4-fluorophenyl)-1-phenylthio-2-(1,2,4-triazol-1-yl)-pentan-3-ol, of melting point 171° C., were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04507141
Source datasetuspto-grants-1985_03
ORD IDord-99ae33feb7214f4ca7d1c2bf55b1b84e
Source noteuspto-grants-1985_03