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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363122Generated: November 1, 2026

HCID 86654777, compound → HCID 67111134, compound

https://huagongshe.com/reaction/2363122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86654777HCID 86654777—
ReactantHCID 178418332HCID 178418332—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67111134HCID 6711113499,950.203%

Reaction Steps

To an ice-cold suspension of 3-(tert-butyl-dimethyl-silanyloxy)-N-methoxy-N-methyl-5-trifluoromethyl-benzamide (500 mg, 1.37 mmol) in THF (5 mL) was added dropwise 3.0M CH3MgCl (687 mL, 2.06 mmol) at 0° C. The mixture was stirred for 3 hours at room temperature, and then diluted with Et2O. The reaction mixture was washed with saturated ammonium chloride, water and brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The crude residue was purified by column chromatography to give 1-[3-(tert-butyl-dimethyl-silanyloxy)-5-trifluoromethyl-phenyl]-ethanone (436 g, 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691855B2
Source datasetuspto-grants-2014_04
ORD IDord-86f8e9e394b24245bcf8f64d42f0826d
Source noteuspto-grants-2014_04