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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587825Generated: October 31, 2026

Methyl trifluoromethyl ketone → HCID 86603896, compound

https://huagongshe.com/reaction/587825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl trifluoromethyl ketoneHCID 9871—
ReactantSodium BicarbonateHCID 516892—
ReactantPotassium hydroxy sulfiteHCID 23707502—
ReactantHCID 68771318HCID 68771318—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 86603896HCID 8660389691%

Reaction Conditions

Temperature0 °C

Reaction Steps

1-Bromo-2,3-dichloro-4-(1-methyl-allyloxy)-benzene (2.5 g), 1,1,1-trifluoroacetone (6.05 mL) and sodium bicarbonate (2.12 g) were taken up in a solvent mixture of acetonitrile and water (2:1, 45 mL) and cooled to 0° C. Oxone (5.19 g) was added in three portions and the reaction was slowly warmed to room temperature. Upon completion the reaction was filtered and concentrated and re-dissolved in ethyl acetate. This solution was washed with saturated NH4Cl, brine and dried over sodium sulfate. Upon filtration, it was concentrated and purified by flash column chromatography eluting with EtOAc in hexanes to get the desired product (2.39 g) in 91% yield as white solid. 1H-NMR (400 MHz, CDCl3) δ: 7.48 (d, 2H), 6.97 (d, 1H), 6.83 (d, 1H), 4.40-4.38 (m, 1H), 4.15-4.08 (m, 1H), 3.25-3.21 (m, 1H), 3.18-3.16 (m, 1H), 2.89 (t, 1H), 2.85-2.68 (m, 3H), 1.49-1.44 (m, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227914B2
Source datasetuspto-grants-2016_01
ORD IDord-3bfa359b22304d5ba83742e0bb059443
Source noteuspto-grants-2016_01