HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874793Generated: October 30, 2026
Methyl trifluoromethyl ketone → HCID 86603896, compound
https://huagongshe.com/reaction/874793
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl trifluoromethyl ketone | HCID 9871 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Reactant | HCID 68771318 | HCID 68771318 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86603896 | HCID 86603896 | 91% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08980950B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-e099950b95ec49f8829d5aaa5877de6c |
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| Source note | uspto-grants-2015_03 |
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