참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | o-(Methylthio)phenol | HCID 61261 | — |
| 반응물 | 3,6-Dichloropyridazine 1-oxide | HCID 260910 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 용매 | Dimethyl Sulfoxide | HCID 679 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 6-Chloro-3-[2-(methylsulfanyl)phenoxy]pyridazine 1-oxide | HCID 22939933 | 56.8% |
반응 단계
In a mixed solvent of 1,4-dioxane (5 mL) and dimethylsulfoxide (5 mL) was dissolved 454 mg (3.24 mmol) of 2-(methylsulfanyl)phenol, to the solution was added 519 mg (4.63 mmol) of potassium tert-butoxide and the mixture was stirred for 35 minutes. To the mixture was added 424 mg (2.57 mmol) of 3,6-dichloropyridazine 1-oxide and the resulting mixture was stirred for 3 hours. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layers were combined, washed with brine, and dried over anhydrous magnesium sulfate. The solvent was removed, and the obtained residue was purified by silica gel chromatography (Wakogel C-100, eluted with hexane:ethyl acetate=3:1) to obtain 391 mg (1.46 mmol, Yield: 56.8%) of 6-chloro-3-[2-(methylsulfanyl)phenoxy]pyridazine 1-oxide.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US07608563B2 |
|---|
| 출처 데이터셋 | uspto-grants-2009_10 |
|---|
| ORD ID | ord-90620fe223434362948d5aa094bb8a12 |
|---|
| 출처 메모 | uspto-grants-2009_10 |
|---|