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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568751Generated: October 29, 2026

Sodium borohydride → HCID 54216095, compound

https://huagongshe.com/reaction/568751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantCalcium ChlorideHCID 5284359—
ReactantHCID 53942418HCID 53942418—
SolventIsopropanolHCID 3776—
ProductHCID 54216095HCID 5421609555%

Reaction Conditions

Temperature25 °C

Reaction Steps

2.0 g (6.13 moles) of the E-isomer of 1-chloro-5-(4-chlorophenyl)-2,2-dimethyl-4-(1,2,4-triazol-1-yl)-4-penten-3-one (the compound of Example 2) and 0.467 g (4.11 mmoles) of calcium chloride were dissolved in 30 ml of isopropanol, and a solution of 0.167 g (4.3 mmoles) of sodium borohydride was added dropwise at -5° C. After 6 hours, the reaction mixture was warmed to 25° C. and concentrated in vacuo. The residue was poured onto water and the mixture was extracted with ethyl acetate. The combined ethyl acetate extracts were dried over sodium sulphate and concentrated in vacuo. The oily residue crystallised on trituration with diisopropyl ether. 1.1 g (55% of theory) of 1-chloro-5-(4-chlorophenyl)-2,2-dimethyl-4-(1,2,4-triazol-1-yl)-4-penten-3-ol of melting point 170° C. were obtained as the E-isomer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04729783
Source datasetuspto-grants-1988_03
ORD IDord-5d54997165ed4de08f83b83cabba304a
Source noteuspto-grants-1988_03