Sodium hydride → 2-(5-Bromo-alpha-cyano-2-methoxymethoxybenzyl)-3-trifluoromethyl-pyridine

HRID 862079노트

반응식

HRID 862079 반응식
[H-].[Na+].[Br:3][C:4]1[CH:5]=[CH:6][C:7]([O:13][CH2:14][O:15][CH3:16])=[C:8]([CH:12]=1)[CH2:9][C:10]#[N:11].Cl[C:18]1[C:23]([C:24]([F:27])([F:26])[F:25])=[CH:22][CH:21]=[CH:20][N:19]=1.C1(C)C=CC(S([O-])=O)=CC=1.[Na+]>CN(C=O)C>[Br:3][C:4]1[CH:5]=[CH:6][C:7]([O:13][CH2:14][O:15][CH3:16])=[C:8]([CH:12]=1)[CH:9]([C:18]1[C:23]([C:24]([F:27])([F:26])[F:25])=[CH:22][CH:21]=[CH:20][N:19]=1)[C:10]#[N:11]

참가 물질

6

실험 절차

Sixty % sodium hydride (656 mg) was added, at room temperature, to a mixture of 5-bromo-2-methoxymethoxybenzyl cyanide (3.50 g), 2-chloro-3-trifluoromethylpyridine (2.48 g), sodium p-toluenesulfinate (731 mg) and DMF (35 ml), followed by stirring for 30 minutes at the same temperature under argon atmosphere. The reaction mixture was poured into an aqueous saline solution, followed by extraction with ethyl acetate. The extract solution was washed with an aqueous saline solution, dried (anhydrous sodium sulfate) and concentrated. The concentrate was purified by means of a silica gel column chromatography (eluent: ethyl acetate/hexane) to give 2-(5-bromo-α-cyano-2-methoxymethoxybenzyl)-3-trifluoromethyl-pyridine (2.63 g) (Compound D-4). The physical properties and spectrum date are shown in Table 13 and Table 14.

후처리

  1. additionThe reaction mixture was poured into an aqueous saline solution
  2. extractionfollowed by extraction with ethyl acetate
  3. washThe extract solution was washed with an aqueous saline solution
  4. dry with materialdried (anhydrous sodium sulfate)
  5. concentrationconcentrated
  6. customThe concentrate was purified by means of a silica gel column chromatography (eluent: ethyl acetate/hexane)

출처 및 근거

ORD 기록
ord-866fbdae74064f1b922de30c2f7a7604
출처 데이터셋
uspto-grants-1998_02
특허 번호
US05716971

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