Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1-(4-Fluorophenyl)-1,3-dihydroisobenzofuran-1-propanol | HCID 19883527 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 19883488 | HCID 19883488 | — |
Reaction Steps
To a stirred solution of 24.2 parts of 1-(4-fluorophenyl)-1,3-dihydroisobenzofuran-1-propanol in 8 parts of pyridine and 90 parts of trichloromethane were added dropwise 12.1 parts of thionyl chloride. Upon completion, the whole was heated slowly to 50° C. and stirring at this temperature was continued for 3 hours. The reaction mixture was poured onto ice-water. The organic phase was separated, washed with a sodium hydrogen carbonate solution (10%), dried and evaporated, yielding 20 parts of 1-(3-chloropropyl)-1-(4-fluorophenyl)-1,3-dihydroisobenzofuran as a residue (intermediate 12).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04766125 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-fe67d16fd2484218ba950edb3088cd79 |
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| Source note | uspto-grants-1988_08 |
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