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Sodium Bicarbonate → 3-(3-Hydroxyphenyl)indoline

HRID 1489149
ノート
印刷プレビュー

反応式

HRID 1489149 の反応式
C[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.ClCCl.B(Br)(Br)Br.C(=O)(O)[O-].[Na+]>ClCCl>[OH: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

5

反応物 3

HCID 516892Sodium BicarbonateHCID 154287243-(3-Methoxyphenyl)indolineHCID 22277759Boron tribromide dichloromethane

生成物 1

HCID 212222863-(3-Hydroxyphenyl)indoline

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

A 3.0 g portion of the (+)-3-(3-methoxyphenyl)indoline obtained in Reference Example 4 was dissolved in 30 ml of dichloromethane, and this solution was added dropwise to 40 ml of a boron tribromide dichloromethane solution (1 mole/liter) at -70° C. After stirring the solution at room temperature overnight, ice water was added, the pH was adjusted to 9 with sodium bicarbonate, and the mixture was extracted with a chloroform/ethanol mixed solvent. After drying and concentration, ether was added to the residue to precipitate crystals which were then collected by filtration to obtain 2.7 g of 3-(3-hydroxyphenyl)indoline.

後処理

  1. additionwas added
  2. extractionthe mixture was extracted with a chloroform/ethanol mixed solvent
  3. customAfter drying
  4. concentrationconcentration, ether
  5. additionwas added to the residue
  6. customto precipitate crystals which
  7. filtrationwere then collected by filtration

出典と根拠

ORDレコード
ord-084dbaa962fd4bae9ca35cf78b2914fb
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