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Dimethyl Sulfoxide → HCID 66919222、化合物

HRID 1673164
ノート
印刷プレビュー

反応式

HRID 1673164 の反応式
Br[CH2:2][CH:3]1[O:8][C:7]2=[CH:9][S:10][CH:11]=[C:6]2[O:5][CH2:4]1.[C:12]([O-:20])(=[O:19])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.[NH4+].CS(C)=O>O>[C:12]([O:20][CH2:2][CH:3]1[CH2:4][O:5][C:6]2=[CH:11][S:10][CH:9]=[C:7]2[O:8]1)(=[O:19])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=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 679Dimethyl SulfoxideHCID 15830Ammonium BenzoateHCID 569236862-(Bromomethyl)-2,3-dihydrothieno[3,4-b][1,4]dioxine

生成物 1

HCID 66919222HCID 66919222、化合物収率 71.1%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

In a 100 mL round bottom flask 9.00 g (0.0382 mol) 2-(bromomethyl)-2,3-dihydrothieno[3,4-b][1,4]dioxine, 6.39 g (0.0459 mol) ammonium benzoate, and 55 g DMSO were combined. A reflux condenser was equipped and the reaction was heated to 100 C overnight. After cooling to room temperature, the reaction mixture was poured into water and the product was extracted with methylene chloride. The organic fractions were combined and the solvent removed under reduced pressure. Purification by column chromatography provided 7.5 g (71% yield) of a white solid whose structure was confirmed by 1H/13C NMR and LC-MS.

後処理

  1. customA reflux condenser was equipped
  2. temperaturethe reaction was heated to 100 C overnight
  3. extractionthe product was extracted with methylene chloride
  4. customthe solvent removed under reduced pressure
  5. customPurification by column chromatography

出典と根拠

ORDレコード
ord-b8eae37cd4ec465db72754e4baedd12e
出典データセット
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07999121B2

反応ノート

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