HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486473Generated: October 29, 2026
Benzyl Alcohol → 3-[4-(3-Methylphenyl)-1-piperazinyl)-6-(phenylmethoxy)pyridazine
https://huagongshe.com/reaction/486473
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 15124568 | HCID 15124568 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-[4-(3-Methylphenyl)-1-piperazinyl)-6-(phenylmethoxy)pyridazine | HCID 15124620 | 47% |
Reaction Steps
To a stirred solution of 0.7 parts of sodium in 20 parts of benzenemethanol were added 5.8 parts of 3-chloro-6-[4-(3-methylphenyl)-1-piperazinyl]pyridazine. The whole was stirred and heated in an oil bath at 180° C. After standing overnight, water was added and the product was extracted with trichloromethane. The extract was dried, filtered and evaporated. 2,2'-Oxybispropane was added to the residue. The product was filtered off and crystallized from a mixture of 2-propanol and methanol. The product was filtered off and dried, yielding 3.4 parts (47%) of 3-[4-(3-methylphenyl)-1-piperazinyl]-6-(phenylmethoxy)pyridazine: mp. 159.4° C. (compound 267).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05292738 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-98eba0aba7e24956bab60f4d8141d20d |
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| Source note | uspto-grants-1994_03 |
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