ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Water → Methyl 3-methoxy-5-(pentafluorosulfanyl)benzoate

HRID 217746
ノート
印刷プレビュー

反応式

HRID 217746 の反応式
[OH:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([S:11]([F:16])([F:15])([F:14])([F:13])[F:12])[CH:10]=1)[C:5](O)=[O:6].IC.[C:19](=O)([O-])[O-].[K+].[K+].O.CN([CH:29]=[O:30])C>>[CH3:19][O:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([S:11]([F:16])([F:15])([F:14])([F:13])[F:12])[CH:10]=1)[C:5]([O:30][CH3:29])=[O:6]
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 5

HCID 962WaterHCID 6228DimethylformamideHCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 581367943-Hydroxy-5-(pentafluorosulfanyl)benzoic acid

生成物 1

HCID 58136953Methyl 3-methoxy-5-(pentafluorosulfanyl)benzoate

実験手順

3-Hydroxy-5-(pentafluorosulfanyl)benzoic acid (O5.007; 3.0 g) was dissolved in absolute DMF (75 ml). Then iodomethane (3.6 ml) was added while stirring, followed by finely powdered potassium carbonate (6.3 g). After stirring at 40° C. for 5 hours, the mixture was cooled and admixed with water (250 ml). The mixture was then extracted four times with ether (100 ml). The combined extracts were each washed once with 1 N sodium hydroxide solution (75 ml) and water (100 ml), dried over magnesium sulfate, filtered and concentrated. 2.9 g of the desired compound were obtained.

後処理

  1. stirringAfter stirring at 40° C. for 5 hours
  2. temperaturethe mixture was cooled
  3. extractionThe mixture was then extracted four times with ether (100 ml)
  4. washeach washed once with 1 N sodium hydroxide solution (75 ml) and water (100 ml)
  5. dry with materialdried over magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated

出典と根拠

ORDレコード
ord-398a2e21a5d54341ba1a5a84a6e96a60
出典データセット
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08198272B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート