반응식
O.O.O.O.O.O.O.O.O.[S-2].[Na+].[Na+].[S].[Br:14][C:15]1[CH:20]=[C:19]([N+:21]([O-:23])=[O:22])[CH:18]=[C:17]([N+:24]([O-:26])=[O:25])[C:16]=1N.[Cl-].[NH4+:29].[OH-].[Na+].Cl>O.C(O)C>[Br:14][C:15]1[CH:20]=[C:19]([N+:21]([O-:23])=[O:22])[C:18]([NH2:29])=[C:17]([N+:24]([O-:26])=[O:25])[CH:16]=1참가 물질
반응 조건
- 온도
- 65 °C
실험 절차
A mixture of sodium sulfide nonahydrate (96 g, 400 mmol) and sulfur (12.8 g, 400 mmol) in a mixture of 400 mL of water and 100 mL of ethanol was heated at reflux under nitrogen for 1 h. The solution was added to a stirred suspension of 2-bromo-4,6-dinitrobenzenamine (104.8 g, 400 mmol) and ammonium chloride (20.8 g, 400 mmol) in a mixture of 400 mL of water and 700 mL of ethanol. The mixture was stirred at 65° C. for 30 min. Then 400 mL of 2N NaOH solution was added dropwise during a period of 30 min and the mixture was then stirred for a further 15 minutes at 65° C. After cooling, the mixture was poured onto a mixture of 2N HCl (400 mL), 1 kg ice and 1 L of water, stirred for 15 min to complete the reaction and extracted with ethyl acetate (1 L×3). The combined organic layers were dried over sodium sulphate and evaporated to give the crude product (90 g, 97%) as a rust-colored solid, which was used for the next step without further purification; LC/MS: MS (ES+) m/e 232 [M+H]+; 1H NMR (300 MHz, DMSO-d6) δ ppm 5.48 (s, 2H), 6.07 (s, 2H), 7.39 (d, J=2.7 Hz, 1H), 7.64 (d, J=2.7 Hz, 1H).
후처리
- temperaturewas heated
- temperatureat reflux under nitrogen for 1 h
- stirringthe mixture was then stirred for a further 15 minutes at 65° C
- temperatureAfter cooling
- stirringstirred for 15 min
- customthe reaction
- extractionextracted with ethyl acetate (1 L×3)
- dry with materialThe combined organic layers were dried over sodium sulphate
- customevaporated
출처 및 근거
- ORD 기록
- ord-ec40050bfb7c43a58c9a5ef6177975fa
- 출처 데이터셋
- uspto-grants-2014_07
- 특허 번호
- US08778937B2
연결된 노트
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