HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543323Generated: October 31, 2026
Sodium borohydride → HCID 13247671, compound
https://huagongshe.com/reaction/543323
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 20206233 | HCID 20206233 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13247671 | HCID 13247671 | 89.2% |
Reaction Steps
In 100 ml of ethanol is dissolved 15.6 g of oily 3-chloro-4-(1-imidazolyl)-2',4',6'-trimethylbenzophenone obtained in the reference example 4. To the ethanol solution is added a solution of 1.8 g of sodium borohydride in 20 ml of water. After the whole solution is stirred at 50° C. for 17 hours, the reaction mixture is poured into ice-cold water and extracted with chloroform. The chloroform is distilled off and the residue is recrystallized from toluene to give 14 g of α-(2,4,6-trimethylphenyl)-3-chloro-4-(1-imidazolyl)benzenemethanol as white crystals, melting at 156°-157° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04661603 |
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| Source dataset | uspto-grants-1987_04 |
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| ORD ID | ord-684fabbd0b814e2984409b36a8c5174f |
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| Source note | uspto-grants-1987_04 |
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