HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296943Generated: October 30, 2026
Boron Trichloride → HCID 178488687, compound
https://huagongshe.com/reaction/1296943
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron Trichloride | HCID 25135 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 58913529 | HCID 58913529 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178488687 | HCID 178488687 | — |
Reaction Steps
5-(2-Benzyloxy-5-chloro-4-fluoro-phenyl)-4-(4-methoxy-phenyl)-3-methyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazole (1 eq) was taken up in anhydrous dichloromethane and the solution was cooled under nitrogen to 0° C. 1M boron trichloride in dichloromethane (6 eq) was added dropwise and the solution was allowed to stir for 1 hour. The reaction mixture was added dropwise to sat. NaHCO3 (aq) and the resulting solution was extracted into dichloromethane. The organic phases were washed with brine, dried over MgSO4, filtered and concentrated in vacuo. The residue was purified by preparative LC/MS, to give 4-chloro-5-fluoro-2-[4-(4-methoxy-phenyl)-5-methyl-2H-pyrazol-3-yl]-phenol as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07247734B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-ef8f3ee3afe949c7932d34e0359ce409 |
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| Source note | uspto-grants-2007_07 |
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