HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370660Generated: October 26, 2026
Sodium borohydride → HCID 3071160, compound
https://huagongshe.com/reaction/370660
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-(4-Diphenylmethylpiperazinyl)-1-(4-hydroxyphenyl)ethanone | HCID 10340129 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 3071160 | HCID 3071160 | 79.2% |
Reaction Steps
In 50 ml of methanol was dissolved 3.0 g (7.8 mmol) of 2-(4-diphenylmethylpiperazinyl)-1-(4-hydroxyphenyl)ethanone, to which 3.0 g (79 mmol) of sodium borohydride was added slowly under ice-cooled conditions. The reaction mixture was then stirred overnight at room temperature, and methanol was removed under reduced pressure. Thereafter, 100 ml of ether was added to the residue, and the solution was washed successively with water and saturated saline and dried over anhydrous sodium sulfate. The resultant ether solution was concentrated, and the residue was purified by silica gel column chromatography (silica gel 90 g; chloroform:methanol=100:1) to give 2.4 g of 2-(4-diphenylmethylpiperazinyl)-1-(4-hydroxyphenyl)ethanol (yield: 79%) which, upon recrystallization from a mixed solvent of ethyl acetate and n-hexane, gave white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04528194 |
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| Source dataset | uspto-grants-1985_07 |
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| ORD ID | ord-afb8743f98e245a082156e60b0db0e78 |
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| Source note | uspto-grants-1985_07 |
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