HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198853Generated: October 26, 2026
Tert-Butylamine → 3-Benzyloxy-1-(tert.butyl)azetidine
https://huagongshe.com/reaction/2198853
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | Benzene, [[2-chloro-1-(chloromethyl)ethoxy]methyl]- | HCID 5155009 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Benzyloxy-1-(tert.butyl)azetidine | HCID 20517332 | 80% |
Reaction Steps
21.9 Parts of 2-benzyloxy-1,3-dichloro-propane, 71.3 parts of tert.-butylamine and 50 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, 17.5 parts of 3-benzyloxy-1-(tert.-butyl)azetidine boiling at 94°-96° C. under 2 mm Hg were obtained. The yield was 80%. The results of infra-red spectrum analysis and nuclear magnetic resonance analysis 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-fd49a4d277ac40b7bcf1fcde0816fe07 |
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| Source note | uspto-grants-1982_11 |
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