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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropylamineHCID 7852—
ReactantBenzene, [[2-chloro-1-(chloromethyl)ethoxy]methyl]-HCID 5155009—
SolventWaterHCID 962—
Product3-Benzyloxy-1-(n-propyl)azetidineHCID 2051733767%

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04018824
Source datasetuspto-grants-1977_04
ORD IDord-c38c256c57644aef8f18d9dcbfef3ddb
Source noteuspto-grants-1977_04