Dimethyl Sulfate → HCID 10773603、化合物

HRID 1039115ノート

反応式

HRID 1039115 の反応式
[F:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([OH:12])=[CH:4][CH:3]=1.[C:13](=O)([O-])[O-].[K+].[K+].S(OC)(OC)(=O)=O>CC(C)=O>[F:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([O:12][CH3:13])=[CH:4][CH:3]=1

参加物

5

反応物 3

HCID 6497Dimethyl SulfateHCID 11430Potassium CarbonateHCID 109208304-fluoronaphthalen-1-ol

生成物 1

HCID 10773603HCID 10773603、化合物収率 48.4%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

21.7 g of 4-Fluoro-naphthalen-1-ol were dissolved in 250 ml acetone. 39.0 g of potassium carbonate and 14.6 ml dimethyl sulphate were added at room temperature. The reaction was placed under nitrogen and stirred for 72 h. The mixture was filtrated; the solid washed with acetone, and the filtrate was concentrated to a viscous oil, which was taken up in ethyl acetate. This was washed with water and with brine, dried over sodium sulphate, filtered through celite and concentrated. The resulting oil was distilled using a Kugelrohr-apparatus, yielding 11.4 g of 4-fluoro-1-methoxynaphthalene.

後処理

  1. filtrationThe mixture was filtrated
  2. washthe solid washed with acetone
  3. concentrationthe filtrate was concentrated to a viscous oil, which
  4. washThis was washed with water and with brine
  5. dry with materialdried over sodium sulphate
  6. filtrationfiltered through celite and
  7. concentrationconcentrated
  8. distillationThe resulting oil was distilled

出典と根拠

ORDレコード
ord-480d342757074fb6ba0c8cc0a47eb99b
出典データセット
uspto-grants-2013_10
特許番号
US08552033B2

反応ノート

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