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Hydrochloric Acid → 3-(3-Methoxyphenyl)indoline

HRID 1489148
ノート
印刷プレビュー

反応式

HRID 1489148 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:9]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[NH:11][CH:10]=2)[CH:6]=[CH:7][CH:8]=1.Cl.[OH-].[Na+]>[Zn].C(O)C>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:9]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[NH:11][CH2:10]2)[CH:6]=[CH:7][CH:8]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 154287153-(3-Methoxyphenyl)indole

生成物 1

HCID 154287243-(3-Methoxyphenyl)indoline収率 48.6%

試薬・触媒・溶媒 2

HCID 23994Zinc触媒HCID 702Ethanol溶媒

実験手順

Ten grams of the abovementioned 3-(3-methoxyphenyl)indole, 700 ml of 6N hydrochloric acid and 300 ml of ethanol were mixed and refluxed while 100 g zinc powder was added in small portions, and then the reflux was continued for 5 hours. The reaction solution was made alkaline with an aqueous sodium hydroxide solution and extracted with chloroform. The resultant extract solution was concentrated to a residue which was then dissolved in diluted hydrochloric acid, and washed with ether. The aqueous layer was made alkaline with sodium hydroxide, extracted with chloroform, and dried and concentrated to obtain 4.9 g of 3-(3-methoxyphenyl)indoline.

後処理

  1. additionwas added in small portions
  2. extractionextracted with chloroform
  3. extractionThe resultant extract solution
  4. concentrationwas concentrated to a residue which
  5. dissolutionwas then dissolved in diluted hydrochloric acid
  6. washwashed with ether
  7. extractionextracted with chloroform
  8. customdried
  9. concentrationconcentrated

出典と根拠

ORDレコード
ord-a8eafaad19b74b64894cde9c44c7ffbc
出典データセット
uspto-grants-1997_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05677326

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート