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Methanol → HCID 73102453、化合物

HRID 2408959
ノート
印刷プレビュー

反応式

HRID 2408959 の反応式
[Cl:1][C:2]([C:7]([CH3:10])([CH3:9])[CH3:8])=[CH:3][C:4]([OH:6])=[O:5].S(Cl)(Cl)=O.O.[CH3:16]O>>[Cl:1][C:2]([C:7]([CH3:10])([CH3:9])[CH3:8])=[CH:3][C:4]([O:6][CH3:16])=[O:5]
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 4

HCID 887MethanolHCID 962WaterHCID 24386Thionyl ChlorideHCID 76219300HCID 76219300、化合物

生成物 1

HCID 73102453HCID 73102453、化合物収率 87%

実験手順

To a solution of 3-chloro-4,4-dimethylpent-2-enoic acid (0.8 g, 4.92 mmol) in methanol (20 mL) was added thionyl chloride (0.714 mL, 9.846 mmol) drop wise under stirring at ice cold temperature. The reaction mixture was refluxed for 2 h and attained to rt. The mixture was poured into ice cooled water and stirred for 15 min. The solution was extracted with chloroform (3×100 mL) and the combined organic layer was washed with water, brine, dried over sodium sulfate and filtered. Solvent was evaporated and the residue was chromatographed over silica gel column using hexane-ethyl acetate (95:5) as eluents to give the product as a pale green color oil (750 mg, 87%). 1H NMR (400 MHz, CDCl3): δ 6.08 (1H, s), 3.75 (3H, s), 1.24 (9H, s).

後処理

  1. temperatureThe reaction mixture was refluxed for 2 h
  2. customattained to rt
  3. additionThe mixture was poured into ice
  4. stirringstirred for 15 min
  5. extractionThe solution was extracted with chloroform (3×100 mL)
  6. washthe combined organic layer was washed with water, brine
  7. dry with materialdried over sodium sulfate
  8. filtrationfiltered
  9. customSolvent was evaporated
  10. customthe residue was chromatographed over silica gel column

出典と根拠

ORDレコード
ord-19b0154d964c4195a440a448a4ea70f6
出典データセット
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08815879B2

反応ノート

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