HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198859Generated: October 26, 2026
Potassium Hydroxide → 1-(2',3'-Dimethyl-4'-methoxyphenoxy)-3-(tert.-butylamino)-2-propanol
https://huagongshe.com/reaction/2198859
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-tert-Butyl-3-hydroxyazetidine | HCID 287986 | — |
| Reactant | 4-Methoxy-2,3-dimethylphenol | HCID 10931625 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 1-(2',3'-Dimethyl-4'-methoxyphenoxy)-3-(tert.-butylamino)-2-propanol | HCID 13055704 | 72.5% |
Reaction Steps
A mixture of 9.1 parts of 2,3-dimethyl-4-methoxyphenol, 6.5 parts of 1-(tert.-butyl)-3-azetidinol and 0.3 part of potassium hydroxide was heated under nitrogen gas at 140° C. for 8 hours with agitation. The reaction product was dissolved in 100 parts of 2 N-hydrochloric acid aqueous solution and washed twice with 100 parts of ether. The water layer was made alkaline with 4 N-sodium hydroxide aqueous solution, and the resulting crystals were recovered by filtration and dried. Then the crystals were dissolved in 100 parts of ether and decolored. The decolored liquid was concentrated and allowed to cool. As a result, 10.2 parts of 1-(2',3'-dimethyl-4'-methoxyphenoxy)-3-(tert.-butylamino)-2-propanol melting at 73°-75° C. were obtained. The yield was 72.5%. The 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-de91f1af25ca4db8b7fe0ee53b575ded |
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| Source note | uspto-grants-1982_11 |
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