Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | Benzene, [[2-chloro-1-(chloromethyl)ethoxy]methyl]- | HCID 5155009 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Benzyloxy-1-ethylazetidine | HCID 20517319 | 61% |
Reaction Steps
21.9 parts of 2-benzyloxy-1,3-dichloro-propane, 45.1 parts of monoethylamine and 45.1 parts of water were added to an autoclave and the mixture was heated at 90° C. for 48 hours with agitation. The reaction mixture was cooled and treated in the same manner as in Example 29, followed by distillation under reduced pressure. As a result, 11.6 parts of 3-benzyloxy-1-ethylazetidine boiling at 73°-74° C. under 2 mm Hg were obtained. The yield was 61%. The results of infra-red spectrum analysis and nuclear magnetic resonance analysis of the product are as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04360464 |
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| Source dataset | uspto-grants-1982_11 |
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| ORD ID | ord-28fec564b1c646919b4cc387725078bd |
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| Source note | uspto-grants-1982_11 |
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