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Methanol → Methyl 3-iodo-2-methylbenzoate

HRID 409230
ノート
印刷プレビュー

反応式

HRID 409230 の反応式
[I:1][C:2]1[C:3]([CH3:11])=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5]([OH:7])=[O:6].S(=O)(=O)(O)O.[CH3:17]O>>[CH3:17][O:6][C:5](=[O:7])[C:4]1[CH:8]=[CH:9][CH:10]=[C:2]([I:1])[C:3]=1[CH3:11]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 887MethanolHCID 1118Sulfuric AcidHCID 27348883-Iodo-2-methylbenzoic acid

生成物 1

HCID 15656853Methyl 3-iodo-2-methylbenzoate

実験手順

A mixture of 3-iodo-2-methyl-benzoic acid (90 mmol, 23.6 g), methanol (250 mL), and concentrated sulfuric acid (13 mL) was refluxed with stirring for 40 h before it was concentrated in vacuo. The residue was dissolved in ethyl acetate and the mixture was neutralized by adding small portions of a saturated aqueous NaHCO3 solution with stirring. The organic phase was dried over MgSO4 and concentrated in vacuo to give the title compound as a yellowish oil (24.3 g); 1H NMR (CDCl3, 200 MHz): δ=7.96 (d, 1H), 7.71 (d, 1H), 6.91 (t, 1H), 3.89 (s, 3H), 2.66 (s, 3H).

後処理

  1. temperaturewas refluxed
  2. concentrationwas concentrated in vacuo
  3. dissolutionThe residue was dissolved in ethyl acetate
  4. additionby adding small portions of a saturated aqueous NaHCO3 solution
  5. stirringwith stirring
  6. dry with materialThe organic phase was dried over MgSO4
  7. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-62ff7fb66780438c9ea20a26d91cb91d
出典データセット
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08759373B2

反応ノート

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