Malonic Acid → (2E)-3-(4-Bromo-2-thienyl)-2-propenoic acid

HRID 1505628ノート

反応式

HRID 1505628 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([CH:7]=O)[S:5][CH:6]=1.N1CCCCC1.C(O)(=O)[CH2:16][C:17]([OH:19])=[O:18]>N1C=CC=CC=1>[Br:1][C:2]1[CH:3]=[C:4](/[CH:7]=[CH:16]/[C:17]([OH:19])=[O:18])[S:5][CH:6]=1

参加物

5

反応条件

温度
100 °C

実験手順

4-Bromothiophenecarboxaldehyde (2.5 g, 13.1 mmol) was placed in a 25 ml round bottomed flask and charged with piperidine (0.14 ml, 0.11 mmol) and pyridine (7.1 ml). Malonic acid was then added (2.21 mg, 21.2 mmol) and the reaction heated to 100° C. and maintained for 24 h. The reaction was then allowed to cool to room temperature and the solvent removed in vacuo. The remaining residue was acidified with concentrated HCl to pH 3 and the solid collected, filtered and washed with distilled water (20 ml). It was then air and oven dried to yield a yellow solid (3.04 g, 100%).

後処理

  1. temperaturemaintained for 24 h
  2. temperatureto cool to room temperature
  3. customthe solvent removed in vacuo
  4. customthe solid collected
  5. filtrationfiltered
  6. washwashed with distilled water (20 ml)
  7. customair and oven dried

出典と根拠

ORDレコード
ord-e00c48da84954c9fa3482e6fb06556eb
出典データセット
uspto-grants-2015_12
特許番号
US09216992B2

反応ノート

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