HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164703Generated: November 1, 2026
Sodium borohydride → HCID 13088604, compound
https://huagongshe.com/reaction/2164703
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 13088594 | HCID 13088594 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 13088604 | HCID 13088604 | 77.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04507141 |
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| Source dataset | uspto-grants-1985_03 |
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| ORD ID | ord-99ae33feb7214f4ca7d1c2bf55b1b84e |
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| Source note | uspto-grants-1985_03 |
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