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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-(Iso-propyl)-3-benzyloxyazetidine | HCID 20517324 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-Phenoxy-2-benzyloxy-3-(iso-propylamino)-propane | HCID 13055706 | 85% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04360464 |
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| Source dataset | uspto-grants-1982_11 |
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| ORD ID | ord-7106f3a59eee4af284823fef7fa7af89 |
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| Source note | uspto-grants-1982_11 |
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