Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromoanisole | HCID 7730 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 23326081 | HCID 23326081 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 23326077 | HCID 23326077 | — |
Reaction Steps
To a stirred and refluxing Grignard complex previously prepared starting from 112.2 parts of 1-bromo-4-methoxybenzene, 15 parts of magnesium and 540 parts of tetrahydrofuran was added dropwise a solution of 84 parts of ethyl 4-(4-fluorobenzoyl)-1-piperidinecarboxylate in 360 parts of tetrahydrofuran. Upon completion, stirring was continued for 2 hours at reflux. After cooling to 10° C., the reaction mixture was poured onto a mixture of 300 parts of crushed ice and 40 parts of acetic acid. The whole was stirred for 5 minutes. 360 Parts of methylbenzene were added. The organic layer was separated, dried, filtered and evaporated, yielding 100 parts of ethyl 4-[(4-fluorophenyl)hydroxy(4-methoxyphenyl)-methyl]-1-piperidinecarboxylate as an oily residue (intermediate 10).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04533665 |
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| Source dataset | uspto-grants-1985_08 |
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| ORD ID | ord-263bd7bfb587402a98ee2e1c73ba261a |
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| Source note | uspto-grants-1985_08 |
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