HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946419Generated: November 3, 2026
Lithium Hexamethyldisilazide → HCID 59547928, compound
https://huagongshe.com/reaction/1946419
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | Benzene, 1-bromo-2-(bromomethyl)-3-(trifluoromethoxy)- | HCID 66770903 | — |
| Reactant | HCID 178522346 | HCID 178522346 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59547928 | HCID 59547928 | — |
Reaction Steps
2,6-difluoro-N-1H-pyrazol-3-ylbenzamide (for a preparation see Intermediate 9)(45 mg, 0.202 mmol) in dry THF (3.0 ml) was stirred under nitrogen at ambient temperature, 1.0 M lithium bis(trimethylsilyl)amide (0.20 ml, 0.20 mmol) was added dropwise and the solution stirred for approximately 90 min then 1-bromo-2-(bromomethyl)-3-[(trifluoromethyl)oxy]benzene (67.3 mg, 1 equiv) in THF (2 ml) was added. The solution was stirred for 5 h then left to stand overnight. The solvent was removed using a stream of nitrogen. To the residue was added aqueous sodium bicarbonate and the mixture was extracted with chloroform three times. The combined organic extracts were filtered through a hydrophobic frit and the filtrate was concentrated in vacuo. The residue was purified by MDAP (Method B). The appropriate fractions were combined and evaporated in vacuo to give the title compound as a white solid (80.6 mg) after drying at high vacuum at 45° C.; LCMS: (System 4) MH+=476, tRET=3.01 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399436B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-59e2e126b90a4cf498dd53d83053f117 |
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| Source note | uspto-grants-2013_03 |
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