Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl bromide | HCID 68176 | — |
| Reactant | HCID 13070378 | HCID 13070378 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 53870913 | HCID 53870913 | 61.8% |
Reaction Steps
Six milliliters (78 millimoles) of thionyl bromide are added to 20 ml of a solution of 5.36 g (32 millimoles) of tricyclo [4.3.1.12,5 ] undecane-1-ol in dry benzene and the entirety is refluxed for 1.5 hours. The reaction mixture is concentrated under reduced pressure and there is further added 20 ml of dry benzene. Reduced pressure concentration is repeated to distill out the excess thionyl chloride completely. The residue is distilled under reduced pressure to collect a fraction boiling at 96°-8° C./2mmHg. Thus 4.53 g (yield 61.3%) of 1-bromotricyclo [4.3.1.12,5 ] undecane are obtained. After cooling, colorless crystals having a melting point of 57.7°-58.5° C. are obtained. The properties of this product are the same as those shown in Example 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04120906 |
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| Source dataset | uspto-grants-1978_10 |
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| ORD ID | ord-71d84457c6d84d6b8966d5c3a010049b |
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| Source note | uspto-grants-1978_10 |
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