HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833843Generated: October 26, 2026
Benzaldehyde → (+/-) 3-alpha-Hydroxybenzylpyridazine
https://huagongshe.com/reaction/1833843
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Pyridazine-3-carboxylic acid | HCID 269369 | — |
| Solvent | P-Cymene | HCID 7463 | — |
| Product | (+/-) 3-alpha-Hydroxybenzylpyridazine | HCID 10397539 | 18.6% |
Reaction Steps
Pyridazine-3-carboxylic acid [prepared as described by Leanza, Becker and Rogers, J.A.C.S., 75, 4086 (1953); 18.6 g.] was mixed with benzaldehyde (44 g.) and p-cymene (360 ml.) and decarboxylated by heating for 3 hours at 135° C. The hot solution was then filtered, cooled and the precipitate collected to give (±) 3-α-hydroxybenzylpyridazine (5.2 g.), m.p. 130°-135° C., in the form of fawn coloured needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04067723 |
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| Source dataset | uspto-grants-1978_01 |
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| ORD ID | ord-e92ba4ad06404f609a6584063ce73fb4 |
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| Source note | uspto-grants-1978_01 |
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