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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButylamineHCID 6385—
ReactantBenzene, [[2-chloro-1-(chloromethyl)ethoxy]methyl]-HCID 5155009—
SolventWaterHCID 962—
Product3-Benzyloxy-1-(tert.butyl)azetidineHCID 2051733280%

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04360464
Source datasetuspto-grants-1982_11
ORD IDord-fd49a4d277ac40b7bcf1fcde0816fe07
Source noteuspto-grants-1982_11