Dimethyl Sulfate → Methyl 2-fluoro-6-iodobenzoate

HRID 243836

反応式

HRID 243836 の反応式
[F:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]([I:11])[C:3]=1[C:4]([OH:6])=[O:5].O[Li].O.S(OC)(O[CH3:19])(=O)=O.[NH4+].[Cl-]>C1COCC1>[CH3:19][O:5][C:4](=[O:6])[C:3]1[C:7]([I:11])=[CH:8][CH:9]=[CH:10][C:2]=1[F:1]

参加物

6

反応条件

温度
50 °C

実験手順

To a 200 mL round-bottomed flask were added 2-fluoro-6-iodo-benzoic acid (7.5 g, 28.2 mmol), LiOH.H2O (1.42 g, 33.8 mmol), and THF (100 mL). The resulting mixture was warmed to 50° C. and stirred for 2 h. Dimethyl sulfate (4.03 mL, 42.3 mmol) was then added and the mixture was warmed to 65° C. After 2 h, the mixture was cooled to room temperature and NH4Cl(aq) (50 mL, 13 wt % solution) was added. The two resulting layers were thoroughly mixed and then separated. The organic layer was dried over MgSO4, filtered, and concentrated under reduced pressure to a light brown oil (7.79 g, 99% yield). 1H NMR (400 MHz, CDCl3): 7.68-7.60 (m, 1H), 7.15-7.06 (m, 2H), 3.98 (s, 3H).

後処理

  1. temperaturethe mixture was warmed to 65° C
  2. waitAfter 2 h
  3. temperaturethe mixture was cooled to room temperature
  4. additionThe two resulting layers were thoroughly mixed
  5. customseparated
  6. dry with materialThe organic layer was dried over MgSO4
  7. filtrationfiltered

出典と根拠

ORDレコード
ord-ba4c3e68549b4aebb9ecf629eb018657
出典データセット
uspto-grants-2014_02
特許番号
US08653263B2

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