Oxalyl chloride → 5,6-Dimethoxy-2-methyl-3-indoleglyoxylyl chloride

HRID 2420518ノート

反応式

HRID 2420518 の反応式
[C:1](Cl)(=[O:5])[C:2]([Cl:4])=[O:3].[CH3:7][O:8][C:9]1[CH:10]=[C:11]2[C:15](=[CH:16][C:17]=1[O:18][CH3:19])[NH:14][C:13]([CH3:20])=[CH:12]2>CCOCC>[CH3:7][O:8][C:9]1[CH:10]=[C:11]2[C:15](=[CH:16][C:17]=1[O:18][CH3:19])[NH:14][C:13]([CH3:20])=[C:12]2[C:1](=[O:5])[C:2]([Cl:4])=[O:3]

参加物

4

反応物 2

HCID 65578Oxalyl chlorideHCID 2665965,6-dimethoxy-2-methyl-1H-indole

生成物 1

HCID 131955395,6-Dimethoxy-2-methyl-3-indoleglyoxylyl chloride

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

8.7 g of oxalyl chloride are added dropwise to a stirring solution, cooled to about -10° C., of 12.0 g of 5,6-dimethoxy-2-methylindole in 250 ml of ether. After addition is complete, the mixture is stirred for 10 minutes, producing a bright orange precipitate of 5,6-dimethoxy-2-methyl-3-indole glyoxylyl chloride which is immediately used for the next step.

後処理

  1. additionAfter addition

出典と根拠

ORDレコード
ord-975019a9bf6f495a8417aecd5b2d7ccf
出典データセット
uspto-grants-1978_08
特許番号
US04110459

反応ノート

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