HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328907Generated: October 30, 2026
Hydrochloric Acid → HCID 12363914, compound
https://huagongshe.com/reaction/328907
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hydroquinone | HCID 785 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-tert-Butyl-3-hydroxyazetidine | HCID 287986 | — |
| Product | HCID 12363914 | HCID 12363914 | 58% |
Reaction Steps
A mixture of 11 parts of hydroquinone, 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 mixture was cooled and dissolved into 50 parts of 4N-hydrochloric acid aqueous solution. The resulting solution was washed with 50 parts of chloroform. The water layer was acidified with concentrated hydrochloric acid, evaporated and solidified. The residue was dissolved in isopropyl alcohol and filtered. The filtrate was decolored with active carbon and allowed to cool. As a result 6.9 parts of 1-(p-hydroxyphenoxy)-3-(tert.-butylamino)-2-propanol hydrochloride melting at 201° - 203° C were obtained. The yield was 58%. The results of infra-red spectrum analysis and nuclear magnetic resonance analysis of the resulting hydrochloride are as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04018824 |
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| Source dataset | uspto-grants-1977_04 |
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| ORD ID | ord-61c3b1a26efd49f291e3f2502cc15091 |
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| Source note | uspto-grants-1977_04 |
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