Sodium Sulfide → HCID 58075503, 화합물

HRID 451011노트

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HRID 451011 반응식
O1CCOCC1.[Cl:7][C:8]1[N:12]=[CH:11][N:10]([C:13]2[CH:18]=[CH:17][C:16]([N+:19]([O-])=O)=[CH:15][C:14]=2[O:22][CH3:23])[N:9]=1.[S-2].[Na+].[Na+]>O>[Cl:7][C:8]1[N:12]=[CH:11][N:10]([C:13]2[CH:18]=[CH:17][C:16]([NH2:19])=[CH:15][C:14]=2[O:22][CH3:23])[N:9]=1

참가 물질

5

반응물 3

HCID 14804Sodium SulfideHCID 312751,4-DioxaneHCID 580757403-chloro-1-(2-methoxy-4-nitrophenyl)-1H-1,2,4-triazole

생성물 1

HCID 58075503HCID 58075503, 화합물수율 73%

시약·촉매·용매 1

HCID 962Water용매2회

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온도
75 °C

실험 절차

Water (8 mL) and dioxane (8 mL) were added to a mixture of 3-chloro-1-(2-methoxy-4-nitrophenyl)-1H-1,2,4-triazole (0.900 g, 3.53 mmol) and sodium sulfide (1.379 g, 17.67 mmol) in a 20 mL vial. The vial was capped and heated at 70-80° C. for 24 hours. The mixture was cooled to rt, poured into water (300 mL) and extracted with EtOAc (2×150 mL). The combined organic layers were washed with brine, dried over sodium sulfate, filtered, and concentrated in vacuo to afford 4-(3-chloro-1H-1,2,4-triazol-1-yl)-3-methoxyaniline (577 mg, 73%) as a brown solid. LC-MS (M+H)+225.1.

후처리

  1. customThe vial was capped
  2. temperatureThe mixture was cooled to rt
  3. extractionextracted with EtOAc (2×150 mL)
  4. washThe combined organic layers were washed with brine
  5. dry with materialdried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-0e1541a2367549d0b5656cc6203cd8e1
출처 데이터셋
uspto-grants-2013_07
특허 번호
US08486952B2

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