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Dimethyl Sulfate → m3OMG

HRID 2213932
ノート
印刷プレビュー

反応式

HRID 2213932 の反応式
O.O.O.O.O.O.O.O.O.O.B([O-])([O-])[O-].[Na+].[Na+].[Na+].[C:18]([O:29][CH3:30])(=[O:28])[C:19]1[CH:27]=[C:25]([OH:26])[C:23]([OH:24])=[C:21]([OH:22])[CH:20]=1.S(OC)(O[CH3:35])(=O)=O.[OH-].[Na+]>O>[OH:26][C:25]1[CH:27]=[C:19]([CH:20]=[C:21]([O:22][CH3:35])[C:23]=1[OH:24])[C:18]([O:29][CH3:30])=[O: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 4

HCID 6497Dimethyl SulfateHCID 7428Methyl GallateHCID 14798Sodium HydroxideHCID 18377803Trisodium;borate;decahydrate

生成物 1

HCID 99622m3OMG収率 85%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

To a stirred mixture of sodium borate decahydrate (borax, 80 g) in H2O (1 L) was added methyl gallate (3, 15.0 g, 82 mmol) at rt. After stirring for 1 h, dimethyl sulfate (30 ml, 317 mmol) and NaOH (50 ml, 6.5 M) were added dropwise simultaneously via separate addition funnels over the course of 1 h. After stirring an additional 12 h, the methylation was terminated with H2SO4, (65 ml, conc.) and stirring continued an additional h. The product was removed by extraction with DCM (5×500 ml, each time stirring the solution for 20 min). The combined DCM extracts were washed with brine (300 ml), dried, concentrated in vacuo, and the residue crystallized from methanol-benzene to afford methyl ether 4 (13.7 g, 85%) as a light tan solid, mp 110–111° C., (lit. mp 110–111° C., Pettit and Singh, 1987); 1H-NMR (300 MHz): 3.89 (3H, s, —OCH3), 3.94 (3H, s, —OCH3), 5.40 (2H, bs, —OH), 5.80 (2H, bs, —OH), 7.22 (1H, d, J=1.8 Hz, ArH), 7.35 (1H, d, J=1.8 Hz, ArH).

後処理

  1. customvia separate
  2. additionaddition funnels over the course of 1 h
  3. stirringAfter stirring an additional 12 h
  4. customthe methylation was terminated with H2SO4, (65 ml, conc.)
  5. stirringstirring
  6. customThe product was removed by extraction with DCM (5×500 ml
  7. stirringeach time stirring the solution for 20 min)
  8. washThe combined DCM extracts were washed with brine (300 ml)
  9. customdried
  10. concentrationconcentrated in vacuo
  11. customthe residue crystallized from methanol-benzene

出典と根拠

ORDレコード
ord-a7ab8c429ced4f2598ed09984a36ad95
出典データセット
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07105695B2

反応ノート

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