Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | HCID 53647688 | HCID 53647688 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 54220385 | HCID 54220385 | — |
Reaction Steps
A 22.4 g (0.067 mole) sample of the 1-bromo-3,3-bis(bromomethyl)-2-azetidinone was dissolved in 450 ml carbon tetrachloride. The insoluble residue (2.0 g) was discarded. A 7 ml (6.07 g, 0.067 mole) portion of toluene was added to the stirred solution. The reaction mixture was irradiated by a 275 watt General Electric Sunlamp and allowed to reflux for one hour. The reaction mixture was decanted hot from a small amount of residue on the stirrer and flask wall and then cooled in ice. White crystals were collected on a filter and dried in vacuo to yield 12.1 g of product. Mother liquor with a few seed crystals was kept cold overnight to yield a second crop of 1.0 g. Total yield of 13.1 g of 76.6% of 3,3-bis(bromomethyl)-2-azetidinone was recovered.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04297475 |
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| Source dataset | uspto-grants-1981_10 |
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| ORD ID | ord-48f914cba45d4f518d80d8b24a066cd7 |
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| Source note | uspto-grants-1981_10 |
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