HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568751Generated: October 29, 2026
Sodium borohydride → HCID 54216095, compound
https://huagongshe.com/reaction/568751
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Calcium Chloride | HCID 5284359 | — |
| Reactant | HCID 53942418 | HCID 53942418 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 54216095 | HCID 54216095 | 55% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04729783 |
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| Source dataset | uspto-grants-1988_03 |
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| ORD ID | ord-5d54997165ed4de08f83b83cabba304a |
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| Source note | uspto-grants-1988_03 |
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