Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198844Generated: October 26, 2026

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

https://huagongshe.com/reaction/2198844

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 2 N-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 numberUS04360464
Source datasetuspto-grants-1982_11
ORD IDord-7106f3a59eee4af284823fef7fa7af89
Source noteuspto-grants-1982_11