HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328900Generated: October 26, 2026
Propylamine → 3-Benzyloxy-1-(n-propyl)azetidine
https://huagongshe.com/reaction/328900
Participants
| Role | Name | HCID | Charge |
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| Reactant | Propylamine | HCID 7852 | — |
| Reactant | Benzene, [[2-chloro-1-(chloromethyl)ethoxy]methyl]- | HCID 5155009 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Benzyloxy-1-(n-propyl)azetidine | HCID 20517337 | 67% |
Reaction Steps
21.9 parts of 2-benzyloxy-1,3-dichloropropane, 59.1 parts of n-propylamine and 59.1 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 13.7 parts of 3-benzyloxy-1-(n-propyl)azetidine boiling at 101° - 103° C. under 2 mm Hg were obtained. The yield was 67%. 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 | US04018824 |
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| Source dataset | uspto-grants-1977_04 |
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| ORD ID | ord-c38c256c57644aef8f18d9dcbfef3ddb |
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| Source note | uspto-grants-1977_04 |
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