Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | AKOS B024490 | HCID 19620032 | — |
| Reactant | HCID 43565332 | HCID 43565332 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86650204 | HCID 86650204 | — |
Reaction Steps
1-(4-Methyl-benzyl)-1H-pyrazole-4-carboxylic acid (0.618 g, 2.86 mmol), which had been prepared according to the protocol described for intermediate (6e), in Example 21, was stirred in toluene (20 mL) at RT and thionyl chloride (681 mg, 0.42 mL, 5.72 mmol) was added. The reaction mixture was slowly heated to 90° C. and heating continued for 3 hrs. After cooling the reaction was concentrated in vacuo. Toluene was added to the residue and concentrated in vacuo. This was repeated a further three times and the crude solid obtained was triturated using isohexane. The solids were separated by filtration washed with isohexane and dried in vacuo to afford 1-(4-methyl-benzyl)-1H-pyrazole-4-carbonyl chloride as a white solid, 0.67 g, quant.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08916591B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-87c384e2a8304abdab9dc93ef907696a |
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| Source note | uspto-grants-2014_12 |
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