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Methanol → Methyl 4-chloro-2-methyl-3-nitrobenzoate

HRID 1161184
ノート
印刷プレビュー

反応式

HRID 1161184 の反応式
[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[C:4]([CH3:11])[C:3]=1[N+:12]([O-:14])=[O:13].[CH3:15]O.S(Cl)(Cl)=O>>[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([O:8][CH3:15])=[O:7])=[C:4]([CH3:11])[C:3]=1[N+:12]([O-:14])=[O:13]
参加物反応条件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 24386Thionyl ChlorideHCID 107039094-Chloro-2-methyl-3-nitrobenzoic acid

生成物 1

HCID 10657064Methyl 4-chloro-2-methyl-3-nitrobenzoate

反応条件

温度
75 °C

実験手順

A round bottom flask was charged with 4-chloro-2-methyl-3-nitrobenzoic acid (11.00 g, 0.05102 mol) and methanol (110 mL, 2.7 mol) and thionyl chloride (4.5 mL, 0.061 mol) was added at 0° C. and the reaction heated at 75° C. for 3 hours. The solvent was removed under reduced pressure and the residue dissolved in ethyl acetate (300 mL) and washed with aqueous sodium bicarbonate, water and brine. The organic extracts were dried over sodium sulfate and the solvent removed to recover the esters. MS m/z=230.3 (M+H).

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート

後処理

  1. additionwas added at 0° C.
  2. customThe solvent was removed under reduced pressure
  3. dissolutionthe residue dissolved in ethyl acetate (300 mL)
  4. washwashed with aqueous sodium bicarbonate, water and brine
  5. dry with materialThe organic extracts were dried over sodium sulfate
  6. customthe solvent removed
  7. customto recover the esters

出典と根拠

ORDレコード
ord-c02916a712bf4fda96931872554bdf30
出典データセット
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07816371B2

反応ノート

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