Methyl iodide → Methyl 3-methylanthranilate

HRID 33752

反応式

HRID 33752 の反応式
[NH2:1][C:2]1[C:10]([CH3:11])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[C:12](=O)([O-])[O-].[Cs+].[Cs+].CI>CN(C)C=O>[NH2:1][C:2]1[C:10]([CH3:11])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([O:6][CH3:12])=[O:5]

参加物

5

実験手順

To a solution of 2-amino-3-methylbenzoic acid (10.1 g, 66.9 mmol) in N,N-dimethylformamide (200 mL) was added cesium carbonate (33.2 g, 102 mmol, 1.5 eq). The mixture was stirred for 30 min. A solution of methyl iodide (4.17 mL, 67.0 mmol, 1.0 eq) in N,N-dimethylformamide (50 mL) was added dropwise and the reaction mixture was maintained for 18 h at rt. The reaction mixture was partitioned between water (1 L) and ether (200 mL) and the water layer was extracted with an additional volume of ether (100 mL). The combined extracts were washed with brine (500 mL), dried over anhydrous potassium carbonate, and concentrated to provide 10.2 g (92%) of methyl 2-amino-3-methylbenzoate. 1H NMR (400 MHz, CDCl3) δ 7.77 (d, 1H), 7.19 (d, 1H), 6.59 (t, 1H), 5.82 (bs, 2H), 3.86 (s, 3H), 2.17 (s, 3H).

後処理

  1. customThe reaction mixture was partitioned between water (1 L) and ether (200 mL)
  2. extractionthe water layer was extracted with an additional volume of ether (100 mL)
  3. washThe combined extracts were washed with brine (500 mL)
  4. dry with materialdried over anhydrous potassium carbonate
  5. concentrationconcentrated

出典と根拠

ORDレコード
ord-44938eae49584069adda697bd7c5e0a6
出典データセット
uspto-grants-2008_09
特許番号
US07429664B2

関連ノート

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