HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842155Generated: October 31, 2026
Sodium borohydride → HCID 10294562, compound
https://huagongshe.com/reaction/842155
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 53786085 | HCID 53786085 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 10294562 | HCID 10294562 | — |
Reaction Steps
To a suspension of 4-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-5-ethoxymethyleneamino-3-trifluoromethylpyrazole (1.0 g) in methanol (10 ml) stirred at room temperature was added sodium borohydride (0.17 g). After 2 hours an additional 0.17 g of sodium borohydride was added, and another 0.34 g added after 1 hours. One hour later the mixture was poured onto water (80 ml). The combined extracts were dried over anhydrous magnesium sulphate, filtered, and evaporated in vacuo. The white solid thus obtained was purified by chromatography on silica (Merck, 230-400 mesh, 0.7 kg cm−2) with dichloromethane as eluent, to furnish 4-cyano-5-methylamino-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-trifluoromethylpyrazole as a white solid )0.6 g), m.p. 200-202° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06372774B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-437acebd07424a4f9dec7cf0c8e026e3 |
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| Source note | uspto-grants-2002_04 |
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