HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 549075Generated: October 27, 2026
Sodium Hydroxide → (1-Methyl-5-phenyl-1H-pyrazol-3-yl)methanol
https://huagongshe.com/reaction/549075
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Calcium Chloride | HCID 5284359 | — |
| Reactant | Ethyl 1-methyl-5-phenyl-1H-pyrazole-3-carboxylate | HCID 7537623 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (1-Methyl-5-phenyl-1H-pyrazol-3-yl)methanol | HCID 14354447 | — |
Reaction Steps
A stirred suspension of sodium borohydride (1.28 g) in dry tetrahydrofuran (80 mL) was treated with calcium chloride (1.88 g). The mixture was stirred for 1 hour then treated with a solution of ethyl 1-methyl-5-phenylpyrazol-3-ylcarboxylate (5.2 g, prepared according to the procedure described by Martins et al., J. Heterocycl. Chem. (1999), 36(1), 217-220) in dry tetrahydrofuran (40 mL). After stirring at room temperature for 3 days and at reflux temperature for 8 hours the mixture was treated with sodium hydroxide solution (50 mL, 1N). This mixture was stirred at room temperature for 1 hour, then evaporated to remove the organic solvents and then extracted three times with dichloromethane (140 mL). The combined extracts were washed with water, then dried over magnesium sulfate and then evaporated to give the title compound as a white solid, m.p. 95-99° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07943616B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-b188177dd96744e1a7102fa6a36c824e |
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| Source note | uspto-grants-2011_05 |
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