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Benzoyl Peroxide → (1S)-2,3,4,6-tetra-O-acetyl-1,5-anhydro-1-[5-(bromomethyl)-2-ethoxyphenyl]-D-glucitol

HRID 1375969
ノート
印刷プレビュー

反応式

HRID 1375969 の反応式
[Br:1]N1C(=O)CCC1=O.C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1.[C:27]([O:30][C@@H:31]1[C@@H:36]([O:37][C:38](=[O:40])[CH3:39])[C@H:35]([O:41][C:42](=[O:44])[CH3:43])[C@@H:34]([CH2:45][O:46][C:47](=[O:49])[CH3:48])[O:33][C@H:32]1[C:50]1[CH:55]=[C:54]([CH3:56])[CH:53]=[CH:52][C:51]=1[O:57][CH2:58][CH3:59])(=[O:29])[CH3:28]>C(Cl)(Cl)(Cl)Cl.C(Cl)(Cl)Cl>[C:27]([O:30][C@@H:31]1[C@@H:36]([O:37][C:38](=[O:40])[CH3:39])[C@H:35]([O:41][C:42](=[O:44])[CH3:43])[C@@H:34]([CH2:45][O:46][C:47](=[O:49])[CH3:48])[O:33][C@H:32]1[C:50]1[CH:55]=[C:54]([CH2:56][Br:1])[CH:53]=[CH:52][C:51]=1[O:57][CH2:58][CH3:59])(=[O:29])[CH3:28]
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 7187Benzoyl PeroxideHCID 67184N-bromobutanimideHCID 58786152(1S)-2,3,4,6-tetra-O-acetyl-1,5-anhydro-1-(2-ethoxy-5-methylphenyl)-D-glucitol

生成物 1

HCID 58786161(1S)-2,3,4,6-tetra-O-acetyl-1,5-anhydro-1-[5-(bromomethyl)-2-ethoxyphenyl]-D-glucitol収率 32.4%

試薬・触媒・溶媒 2

HCID 5943
Carbon Tetrachloride
溶媒
HCID 6212Chloroform溶媒

実験手順

N-bromosuccinimide (1.7 g) and benzoyl peroxide (0.1 g) were added to a solution of (1S)-2,3,4,6-tetra-O-acetyl-1,5-anhydro-1-(2-ethoxy-5-methylphenyl)-D-glucitol (3.7 g) in carbon tetrachloride (30.0 ml) and the mixture was refluxed with heating for one hour. The reaction mixture was diluted with chloroform and the diluted product was washed with saturated aqueous solution of sodium hydrogencarbonate, saturated aqueous solution of sodium thiosulfate, and saturated brine in that order and dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated. The resulting precipitates were collected by filtration to obtain (1S)-2,3,4,6-tetra-O-acetyl-1,5-anhydro-1-[5-(bromomethyl)-2-ethoxyphenyl]-D-glucitol (1.4 g).

後処理

  1. temperaturethe mixture was refluxed
  2. temperaturewith heating for one hour
  3. washthe diluted product was washed with saturated aqueous solution of sodium hydrogencarbonate, saturated aqueous solution of sodium thiosulfate, and saturated brine in that order
  4. dry with materialdried over anhydrous sodium sulfate
  5. filtrationAfter filtration
  6. concentrationthe filtrate was concentrated
  7. customThe resulting precipitates
  8. filtrationwere collected by filtration

出典と根拠

ORDレコード
ord-72b32baac77549a68697199466f8ae00
出典データセット
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07169761B2

反応ノート

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