HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49675Generated: October 31, 2026
Water → 3-Chloro-2-methyl-6-methylsulfonylbenzaldoxime
https://huagongshe.com/reaction/49675
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Butyl nitrite | HCID 10996 | — |
| Reactant | HCID 18757270 | HCID 18757270 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Chloro-2-methyl-6-methylsulfonylbenzaldoxime | HCID 73461943 | — |
Reaction Steps
A solution of 12.7 g (119 mmol) of n-butyl nitrite (97% pure) and 20 g (92 mmol) of 2,3-dimethyl-4-methylsulfonylchlorobenzene in 100 ml of dimethylformamide is cooled to from −55 to −60° C., and a solution of 16.8 g (147 mmol) of potassium tert-butoxide in 70 ml of dimethylformamide is added dropwise at this temperature, over a period of 30 minutes. The reaction is monitored by HPLC. For work-up, initially 50 ml of water are added, and the pH is subsequently adjusted to 5-6 using approximately 30 ml of glacial acetic acid. The reaction mixture is subsequently poured into 0.7 kg of ice-water, and the aqueous phase is extracted with methylene chloride. The organic phase is washed with sodium bicarbonate solution, dried over magnesium sulfate and concentrated. This gives 18.4 g of a light-beige crude product which is purified by recrystallization from approximately 30 ml of toluene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06706886B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-5ea4bc75f9f648a18d19f8443d30ff76 |
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| Source note | uspto-grants-2004_03 |
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