HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579247Generated: October 30, 2026
Tetrahydrofuran → 1-[2-(1,3,5-Triethylphenyl)-2-oxoacetyl]-1-methyl-2-(1-methylsulfonyl-2-propylidene)hydrazine
https://huagongshe.com/reaction/579247
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Methyl-2-(1-methylsulfonyl-2-propylidene)hydrazine | HCID 76468959 | — |
| Reactant | 2-(1,3,5-Triethylphenyl)-2-oxoacetyl chloride | HCID 86689351 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 1-[2-(1,3,5-Triethylphenyl)-2-oxoacetyl]-1-methyl-2-(1-methylsulfonyl-2-propylidene)hydrazine | HCID 86689352 | 75% |
Reaction Steps
To a 3 L volume four-necked flask, 1-methyl-2-(1-methylsulfonyl-2-propylidene)hydrazine (5-2-1) (116.0 g), tetrahydrofuran (anhydrous) (600 ml), and triethylamine (98.5 ml) were added under a nitrogen atmosphere, and cooled to about 1° C. to the mixture, 2-(1,3,5-triethylphenyl)-2-oxoacetyl chloride (6-b) (178.5 g) was added dropwise, and stirred at 0° C. for 1 hour. The reaction mixture was added dropwise to hexane (3 L) at room temperature, and stirred for 1 hour. The precipitated solids were collected by filtration, washed with hexane (0.5 L×2) and water (0.5 L×6), and dried under reduced pressure to give 200.9 g of 1-[2-(1,3,5-triethylphenyl)-2-oxoacetyl]-1-methyl-2-(1-methylsulfonyl-2-propylidene)hydrazine ((4-34)-(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-43e4446a82624c0db6641edec0cbda45 |
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| Source note | uspto-grants-2015_05 |
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