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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946419Generated: November 3, 2026

Lithium Hexamethyldisilazide → HCID 59547928, compound

https://huagongshe.com/reaction/1946419

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantBenzene, 1-bromo-2-(bromomethyl)-3-(trifluoromethoxy)-HCID 66770903—
ReactantHCID 178522346HCID 178522346—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59547928HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399436B2
Source datasetuspto-grants-2013_03
ORD IDord-59e2e126b90a4cf498dd53d83053f117
Source noteuspto-grants-2013_03