Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 20215998 | HCID 20215998 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 12962152 | HCID 12962152 | — |
Reaction Steps
2-Chloro-11-hydroxy-6,11-dihydrodibenz[b,e]oxepin (12.75 g; 0.051 mole) is dissolved in dry ether (220 ml) and cooled to 5° C. under a dry nitrogen atmosphere. Thionyl chloride (6.76 g; 0.056 mole) in ether (20 ml) is slowly added dropwise while maintaining the temperature below 5° C. Upon completion of the addition, the reaction is brought to ambient temperature and stirred for three hours. Upon removal of the solvent in vacuo, the resulting solid is recrystallized from cyclohexane to give crystals of 2,11-dichloro-6,11-dihydrodibenz[b,e]oxepin, m.p. 125°-127° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04335122 |
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| Source dataset | uspto-grants-1982_06 |
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| ORD ID | ord-34c66a6721234c46b2223aa4548d11c4 |
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| Source note | uspto-grants-1982_06 |
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