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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487129Generated: October 30, 2026

tert-Butyldimethylsilyl trifluoromethanesulphonate → HCID 57214691, compound

https://huagongshe.com/reaction/1487129

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyldimethylsilyl trifluoromethanesulphonateHCID 123564—
ReactantHCID 23336273HCID 23336273—
SolventTolueneHCID 1140—
ProductHCID 57214691HCID 5721469137.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

Under nitrogen atmosphere, (tert-butyl)-2-(3-nitrophenyl)-2-oxoacetamide (1.50 g, 5.99 mmol) was taken in toluene (10 ml) at room temperature, tert-butyldimethylsilyl trifluoromethane sulfonate (1.378 ml, 5.99 mmol) was added and the reaction mixture was heated at 100° C. for 8 hrs. The reaction mixture was concentrated under vacuum and satd. sodium bicarbonate solution was added, the mixture was extracted with ethyl acetate (3×20 ml). Combined organic layer was dried over sodium sulfate and the mixture was concentrated under vacuum to afford the crude product, which was purified by column chromatography to afford yellow solid product (440 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428499B2
Source datasetuspto-grants-2016_08
ORD IDord-012034268fdb4980b11d96f1742ec650
Source noteuspto-grants-2016_08