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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328894Generated: October 25, 2026

Phenol → 1-Phenoxy-2-benzyloxy-3-(iso-propylamino)-propane

https://huagongshe.com/reaction/328894

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantPotassium HydroxideHCID 14797—
Reactant1-(Iso-propyl)-3-benzyloxyazetidineHCID 20517324—
SolventDiethyl EtherHCID 3283—
Product1-Phenoxy-2-benzyloxy-3-(iso-propylamino)-propaneHCID 1305570685%

Reaction Conditions

Temperature180 °C

Reaction Steps

To a mixture of 6.2 parts of 1-(iso-propyl)-3-benzyloxyazetidine and 28 parts of phenol 1.5 parts of potassium hydroxide was added, and the mixture was heated at 180° C. for 6 hours. The reaction mixture was cooled and 100 parts of ether were added thereto. The excessive phenol was extracted with 2N-sodium hydroxide aqueous solution and removed. The remaining ether layer was washed in water and dried over anhydrous sodium sulfate. After distillation of ether, the residue was successively subjected to distillation to yield 7.6 parts of 1-phenoxy-2-benzyloxy-3-(iso-propylamino)-propane boiling at 158°-160° C. under 2 mm Hg. The yield was 85%. 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-bf2230889b2349638c581d5f3756713c
Source noteuspto-grants-1977_04