HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436902Generated: October 30, 2026
HCID 178469914, compound → HCID 178519878, compound
https://huagongshe.com/reaction/436902
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 178469914 | HCID 178469914 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178519878 | HCID 178519878 | — |
Reaction Steps
A solution of 12 g of ethyl-(4-chloro-phenyl-4-ethoxycarbonyl-pyrazole in 150 ml of tetrahydrofuran is cooled in an ice bath. Then 25 ml of a 1 molar solution of aluminum hydride triethylamine complex in benzene is added dropwise. After the addition, the ice bath is removed and the gelatinous mixture stirred at room temperature for 21/2 hours. Excess reagent is then destroyed by the dropwise addition of water followed by 30 ml of an aqueous 2N solution of sodium hydroxide. The layers are separated, the aqueous phase reextracted with ethyl acetate and the combined organic layers dried over anhydrous sodium sulfate. The recrystallization of the solid residue from hot ethyl acetate gives the 3-(4-chloro-phenyl)-4-hydroxymethyl-pyrazole, m.p. 149°-150°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04028381 |
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| Source dataset | uspto-grants-1977_06 |
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| ORD ID | ord-596db95e7d204302a02a3a31a9678c64 |
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| Source note | uspto-grants-1977_06 |
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