Thionyl Chloride → (3,4-dihydro-6-methoxy-2,5,7,8-tetramethyl-2H-benzopyran-2-yl)acetyl chloride

HRID 568734

反応式

HRID 568734 の反応式
[CH3:1][O:2][C:3]1[C:4]([CH3:20])=[C:5]([CH3:19])[C:6]2[O:11][C:10]([CH2:13][C:14](O)=[O:15])([CH3:12])[CH2:9][CH2:8][C:7]=2[C:17]=1[CH3:18].S(Cl)([Cl:23])=O>CN(C)C=O.C1C=CC=CC=1>[CH3:1][O:2][C:3]1[C:4]([CH3:20])=[C:5]([CH3:19])[C:6]2[O:11][C:10]([CH2:13][C:14]([Cl:23])=[O:15])([CH3:12])[CH2:9][CH2:8][C:7]=2[C:17]=1[CH3:18]

参加物

5

反応物 2

HCID 24386Thionyl ChlorideHCID 14210610(3,4-dihydro-6-methoxy-2,5,7,8-tetramethyl-2H-benzopyran-2-yl)acetic acid

生成物 1

HCID 20150413(3,4-dihydro-6-methoxy-2,5,7,8-tetramethyl-2H-benzopyran-2-yl)acetyl chloride

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide触媒HCID 241Benzene溶媒

実験手順

To a solution composed of 3.34 g of (3,4-dihydro-6-methoxy-2,5,7,8-tetramethyl-2H-benzopyran-2-yl)acetic acid, 2 drops of N,N-dimethylformamide and 50 ml of benzene was added 0.87 ml of thionyl chloride, and the mixture was refluxed for 2 hours. After cooling, the reaction mixture was evaporated under reduced pressure to remove the low-boiling substances. The above procedure gave (3,4-dihydro-6-methoxy-2,5,7,8-tetramethyl-2H-benzopyran-2-yl)acetyl chloride in a quantitative yield of 3.56 g.

後処理

  1. temperaturethe mixture was refluxed for 2 hours
  2. temperatureAfter cooling
  3. customthe reaction mixture was evaporated under reduced pressure
  4. customto remove the low-boiling substances

出典と根拠

ORDレコード
ord-16671876f3c044feb20c49734e758072
出典データセット
uspto-grants-1988_03
特許番号
US04728650

関連ノート

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