Water → 3-Bromobenzophenone

HRID 45451

反応式

HRID 45451 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Li]C(C)(C)C.Br[C:14]1[CH:15]=[C:16]([CH:22]=[CH:23][CH:24]=1)[C:17](N(C)C)=[O:18].O>C1COCC1.CCCCC>[Br:1][C:2]1[CH:7]=[C:6]([C:17]([C:16]2[CH:22]=[CH:23][CH:24]=[CH:14][CH:15]=2)=[O:18])[CH:5]=[CH:4][CH:3]=1

参加物

7

反応条件

温度
-80 °C

実験手順

To a solution of 8.25 g (52.5 mmol) of bromobenzene in 100 mL of THF, 70 mL (105 mmol) of 2.5 M tBuLi in pentane was added dropwise with vigorous stirring for 2 h at −80° C. This mixture was slowly warmed to room temperature and then stirred for 30 min at this temperature. 11.4 g (50 mmol) of 3-bromo-N,N-dimethylbenzamide was added at 0° C., and the resulting mixture was stirred for 12 hr at room temperature. 150 mL of water was added, the organic solvent was evaporated using a rotary evaporator, and the product was extracted with 2×100 mL of dichloromethane. The combined extracts were dried over K2CO3 and then evaporated to dryness. This procedure gave 12.2 g (89%) of 16 which was further used without an additional purification.

後処理

  1. temperatureThis mixture was slowly warmed to room temperature
  2. stirringstirred for 30 min at this temperature
  3. stirringthe resulting mixture was stirred for 12 hr at room temperature
  4. customthe organic solvent was evaporated
  5. customa rotary evaporator
  6. extractionthe product was extracted with 2×100 mL of dichloromethane
  7. dry with materialThe combined extracts were dried over K2CO3
  8. customevaporated to dryness

出典と根拠

ORDレコード
ord-bb629087c8004f54a980293da4baaddd
出典データセット
uspto-grants-2013_09
特許番号
US08541522B2

関連ノート

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