9-Anthracenecarboxylic acid → Anthracene-9-carbonyl chloride

HRID 489888

反応式

HRID 489888 の反応式
[CH:1]1[C:14]2[C:5](=[CH:6][C:7]3[C:12]([C:13]=2[C:15]([OH:17])=O)=[CH:11][CH:10]=[CH:9][CH:8]=3)[CH:4]=[CH:3][CH:2]=1.C(Cl)(Cl)[Cl:19]>S(Cl)(Cl)=O>[CH:1]1[C:14]2[C:5](=[CH:6][C:7]3[C:12]([C:13]=2[C:15]([Cl:19])=[O:17])=[CH:11][CH:10]=[CH:9][CH:8]=3)[CH:4]=[CH:3][CH:2]=1

参加物

4

反応物 2

HCID 22019-Anthracenecarboxylic acidHCID 6212Chloroform

生成物 1

HCID 167528Anthracene-9-carbonyl chloride収率 59%

試薬・触媒・溶媒 1

HCID 24386Thionyl Chloride溶媒

実験手順

Anthracene-9-carboxylic acid (recrystallized from ethanol, 12.05 g, 54.3 mmol) was suspended in a mixture of chloroform (60 mL, Aldrich, amylenes-stabilized) and thionyl chloride (12 mL) and heated under reflux until a clear solution was obtained (about 30 minutes). The solvent was removed by distillation under reduced pressure and the residual hot oil was dissolved in toluene (20 mL) and hexane (100 mL) was added. After cooling to ambient temperature the crystalline product was collected by filtration and dried in a stream of nitrogen then under high vacuum to give the title compound as a yellow solid (7.69 g, 59%). Non-commercially available carboxylic acids referred to in this section were prepared as described below. If desired they were converted to the corresponding carbonyl chloride using thionyl chloride as described above.

後処理

  1. temperatureheated
  2. temperatureunder reflux until a clear solution
  3. customwas obtained (about 30 minutes)
  4. customThe solvent was removed by distillation under reduced pressure
  5. dissolutionthe residual hot oil was dissolved in toluene (20 mL)
  6. additionhexane (100 mL) was added
  7. filtrationwas collected by filtration
  8. customdried in a stream of nitrogen

出典と根拠

ORDレコード
ord-6d6df2e26fae423f9920d14f54d9331b
出典データセット
uspto-grants-2005_12
特許番号
US06979741B2

関連ノート

読み込み中…