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Dimethyl Sulfate → 1,3-Dimethoxynaphthalene

HRID 1353978
ノート
印刷プレビュー

反応式

HRID 1353978 の反応式
[OH:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[C:4](O)[CH:3]=1.[C:13](=[O:16])([O-])[O-].[K+].[K+].S(OC)(O[CH3:23])(=O)=O.[OH-].[Na+]>CC(C)=O>[CH3:23][O:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[C:4]([O:16][CH3:13])[CH:3]=1
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 86011,3-DihydroxynaphthaleneHCID 11430Potassium CarbonateHCID 14798Sodium Hydroxide

生成物 1

HCID 8707561,3-Dimethoxynaphthalene収率 85.1%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

To 1,3-Dihydroxynaphthalene (15 g, 93.6 mmol) and potassium carbonate (20 g, 144.7 mmol) in acetone (200 ml) was added dimethyl sulfate (21 ml, 222 mmol). After stirring over-night the reaction mixture was mixed with 10% sodium hydroxide (100 ml) and extracted with ethyl acetate (200 ml×2) The organic layer was washed with water (100 ml×2) evaporated, and the residue stirred with ammonium hydroxide (50 ml) for 2 hrs to quench any unreacted dimethyl sulfate. Product was extracted with ethyl acetate (200 ml) and was washed with water (100 ml×2) and brine (100 ml). The solvent was evaporated yielding 15 g (85%) of 6.

後処理

  1. extractionextracted with ethyl acetate (200 ml×2) The organic layer
  2. washwas washed with water (100 ml×2)
  3. customevaporated
  4. stirringthe residue stirred with ammonium hydroxide (50 ml) for 2 hrs
  5. customto quench any unreacted dimethyl sulfate
  6. extractionProduct was extracted with ethyl acetate (200 ml)
  7. washwas washed with water (100 ml×2) and brine (100 ml)
  8. customThe solvent was evaporated

出典と根拠

ORDレコード
ord-0c83842825774209864d0faa67ec850e
出典データセット
uspto-grants-2007_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
USRE039663E1

反応ノート

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