HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579237Generated: October 30, 2026
Water → 1-[2-(2,4,6-Triethylphenyl)-2-oxoacetyl]-2-(1,1,1-trifluoro-3-methylsulfanyl-2-propylidene)-1-methylhydrazine
https://huagongshe.com/reaction/579237
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 1,1,1-Trifluoro-3-methylsulfanyl-2-propanone | HCID 14064749 | — |
| Reactant | 1-[2-(2,4,6-Triethylphenyl)-2-oxoacetyl]-1-methylhydrazine | HCID 66695561 | — |
| Catalyst | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-[2-(2,4,6-Triethylphenyl)-2-oxoacetyl]-2-(1,1,1-trifluoro-3-methylsulfanyl-2-propylidene)-1-methylhydrazine | HCID 76469026 | 50% |
Reaction Steps
To a 100 ml volume three-necked flask, 1-[2-(2,4,6-triethylphenyl)-2-oxoacetyl]-1-methylhydrazine ((12-2)-(11)-40) (3.01 g) was added, and to the mixture was added dropwise a solution of 1,1,1-trifluoro-3-methylsulfanyl-2-propanone (7-0-2) (2.10 g) in toluene (27 g), followed by the addition of para-toluenesulfonic acid monohydrate (0.030 g). The resulting mixture was stirred under reflux for 40 minutes. Then, the reaction mixture was cooled to room temperature, poured into water (30 ml), and extracted with ethyl acetate (50 ml) 3 times. The resulting organic layer was dried over magnesium sulfate, concentrated under reduced pressure, and subjected to silica gel column chromatography (chloroform) to give 2.31 g of 1-[2-(2,4,6-triethylphenyl)-2-oxoacetyl]-2-(1,1,1-trifluoro-3-methylsulfanyl-2-propylidene)-1-methylhydrazine ((4-46)-(1)-40).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040709B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-58b2000c0a1f4075a5e72ea6b7fc8253 |
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| Source note | uspto-grants-2015_05 |
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