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Methyl iodide → HCID 22101417, 화합물

HRID 1457947
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HRID 1457947 반응식
[Br:1][C:2]1[CH:10]=[C:9]([F:11])[C:8]([S:12]([CH3:15])(=[O:14])=[O:13])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].CI.[C:18](=O)([O-])[O-].[K+].[K+]>CN(C=O)C>[Br:1][C:2]1[CH:10]=[C:9]([F:11])[C:8]([S:12]([CH3:15])(=[O:14])=[O:13])=[CH:7][C:3]=1[C:4]([O:6][CH3:18])=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 221013972-Bromo-4-fluoro-5-methylsulphonylbenzoic acid

생성물 1

HCID 22101417HCID 22101417, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

5.8 g of 2-bromo-4-fluoro-5-methylsulphonylbenzoic acid are stirred, at room temperature for 12 h, in 20 ml of DMF together with 3.7 ml of methyl iodide and 8.3 g of potassium carbonate. The reaction mixture is then concentrated and 50 ml of water are added to it. The resulting precipitate is filtered off with suction and dried. Methyl 2-bromo-4-fluoro-5-methylsulphonylbenzoate is obtained, m.p. 126°.

후처리

  1. concentrationThe reaction mixture is then concentrated
  2. addition50 ml of water are added to it
  3. filtrationThe resulting precipitate is filtered off with suction
  4. customdried

출처 및 근거

ORD 기록
ord-e7e81265df5449dca25d05449d7eb82e
출처 데이터셋
uspto-grants-1998_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05849796

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