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Water → 1-[2-(Acetylamino)ethyl]-6-hydroxyindan

HRID 1978016
ノート
印刷プレビュー

反応式

HRID 1978016 の反応式
[C:1]([NH:4][CH2:5][CH2:6][CH:7]1[C:15]2[C:10](=[CH:11][CH:12]=[C:13]([O:16]C)[CH:14]=2)[CH2:9][CH2:8]1)(=[O:3])[CH3:2].B(Br)(Br)Br.O>ClCCl>[C:1]([NH:4][CH2:5][CH2:6][CH:7]1[C:15]2[C:10](=[CH:11][CH:12]=[C:13]([OH:16])[CH:14]=2)[CH2:9][CH2:8]1)(=[O:3])[CH3:2]
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 962WaterHCID 25134Boron tribromideHCID 155239391-[2-(Acetylamino)ethyl]-6-methoxyindan

生成物 1

HCID 219168881-[2-(Acetylamino)ethyl]-6-hydroxyindan収率 78.2%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a solution of 1-[2-(acetylamino)ethyl]-6-methoxyindan (6.40 g, 27.4 mmol) in dichloromethane (150 ml) was added dropwise, under ice-cooling, boron tribromide (5.19 ml, 54.8 mmol). The mixture was then stirred for one hour. The reaction mixture was poured into water. The mixture was stirred for 8 hours at room temperature, which was subjected to extraction with chloroform. The extract solution was washed with brine, which was dried over anhydrous magnesium sulfate, followed by distilling off the solvent under reduced pressure. The residue was recrystallized from ethyl acetate/isopropyl ether to give 4.70 g (yield 78%) of the above-titled compound, m.p.107-108° C.

後処理

  1. temperaturecooling
  2. stirringThe mixture was stirred for 8 hours at room temperature
  3. extractionwhich was subjected to extraction with chloroform
  4. washThe extract solution was washed with brine, which
  5. dry with materialwas dried over anhydrous magnesium sulfate
  6. distillationby distilling off the solvent under reduced pressure
  7. customThe residue was recrystallized from ethyl acetate/isopropyl ether

出典と根拠

ORDレコード
ord-628e5fe3c26947a291469c14e60c6528
出典データセット
uspto-grants-2001_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06235789B1

反応ノート

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