HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 364773Generated: October 26, 2026
Ammonium Chloride → 1-(4-Fluorophenyl)-1-(4-benzyloxyphenyl)-propan-1-ol
https://huagongshe.com/reaction/364773
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-Fluoro-4'-benzyloxy-benzophenone | HCID 20239868 | — |
| Reactant | HCID 178506846 | HCID 178506846 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-(4-Fluorophenyl)-1-(4-benzyloxyphenyl)-propan-1-ol | HCID 20239877 | — |
Reaction Steps
To 125 ml. of a 0.8 molar ethereal ethyl lithium solution a solution of 12.25 g. of 4-fluoro-4'-benzyloxy-benzophenone in 180 ml. of dry ether is added dropwise, in argon atmosphere, with stirring at -20° C. The reaction mixture is allowed to warm up to room temperature and stirred for further 90 minutes. It is then poured into saturated aqueous ammonium chloride solution under cooling. The aqueous phase is extracted with ether, the organic phases are combined and washed to neutral with water. After drying over anhydrous magnesium sulfate ether is distilled off under reduced pressure. The solid residue is crystallized from a mixture of ethyl acetate and n-heptane to yield 7.4 g. of the named compound, melting at 56°-57° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04605785 |
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| Source dataset | uspto-grants-1986_08 |
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| ORD ID | ord-7da82f9233394934af5031081598d31a |
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| Source note | uspto-grants-1986_08 |
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