Dimethyl Sulfone → 1-(3-Ethoxy-4-methoxyphenyl)-2-(methylsulfonyl)ethenamine

HRID 55932

反応式

HRID 55932 の反応式
[CH3:1][S:2]([CH3:5])(=[O:4])=[O:3].C([Li])CCC.CCCCCC.[CH2:17]([O:19][C:20]1[CH:21]=[C:22]([CH:25]=[CH:26][C:27]=1[O:28][CH3:29])[C:23]#[N:24])[CH3:18]>C1COCC1.O>[CH2:17]([O:19][C:20]1[CH:21]=[C:22]([C:23]([NH2:24])=[CH:1][S:2]([CH3:5])(=[O:4])=[O:3])[CH:25]=[CH:26][C:27]=1[O:28][CH3:29])[CH3:18]

参加物

7

反応条件

温度
27.5 °C

実験手順

A slurry of dimethylsulfone (85 g, 903 mmol) in THF (480 ml) was treated with a 1.6M solution of n-butyllithium in hexane (505 ml, 808 mmol) at 0-5° C. The resulting mixture was agitated for 1 hour then a solution of 3-ethoxy-4-methoxybenzonitrile (80 g, 451 mmol) in THF (240 ml) was added at 0-5° C. The mixture was agitated at 0-5° C. for 0.5 hour, warmed to 25-30° C. over 0.5 hour and then agitated for 1 hour. Water (1.4 L) was added at 25-30° C. and the reaction mass was agitated overnight at room temperature (20-30° C.). The solid was filtered and subsequently washed with a 2:1 mixture of water:THF (200 ml), water (200 ml) and heptane (2×200 ml). The solid was dried under reduced pressure at 40-45° C. to provide the product as a white solid (102 g, 83% yield); 1H NMR (DMSO-d6) δ 1.34 (t, J=7.0 Hz, 3H), 2.99 (s, 3H), 3.80 (s, 3H), 4.08 (q, J=7.0 Hz, 2H), 5.03 (s, 1H), 6.82 (s, 2H), 7.01 (d, J=8.5 Hz, 1H), 7.09-7.22 (m, 2H).

後処理

  1. stirringThe mixture was agitated at 0-5° C. for 0.5 hour
  2. stirringagitated for 1 hour
  3. stirringthe reaction mass was agitated overnight at room temperature (20-30° C.)
  4. filtrationThe solid was filtered
  5. washsubsequently washed with a 2:1 mixture of water
  6. customThe solid was dried under reduced pressure at 40-45° C.

出典と根拠

ORDレコード
ord-f3357c3e07c34d3ba3fecb7c78a96830
出典データセット
uspto-grants-2016_09
特許番号
US09434689B2

関連ノート

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