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Methanol → Methyl 3-methylpyrazine-2-carboxylate

HRID 930457
ノート
印刷プレビュー

反応式

HRID 930457 の反応式
[CH3:1][C:2]1[C:3]([C:8]([OH:10])=[O:9])=[N:4][CH:5]=[CH:6][N:7]=1.S(=O)(=O)(O)O.[CH3:16]O>>[CH3:1][C:2]1[C:3]([C:8]([O:10][CH3:16])=[O:9])=[N:4][CH:5]=[CH:6][N:7]=1
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 1118Sulfuric AcidHCID 131534683-Methylpyrazine-2-carboxylic acid

生成物 1

HCID 13153469Methyl 3-methylpyrazine-2-carboxylate収率 73%

反応条件

温度
80 °C

実験手順

In a 2-L flask, 3-methylpyrazine-2-carboxylic acid (Matrix, 19.95 g, 144 mmol) was suspended in MeOH (500 mL). The suspension was cooled in an ice-water bath, and concentrated sulfuric acid (Fluka, 27.3 mL, 506 mmol) was added over a time period of 5 min. The reaction mixture was heated to 80° C. for 5 h. The reaction mixture was concentrated under reduced pressure and the residue was taken up in DCM (750 mL). The excess acid was neutralized carefully with aqueous NaOH (5m, 200 mL). The aqueous layer was separated and extracted with DCM (250 mL). The combined organic layers were combined, dried over MgSO4 and concentrated to afford 16.15 g of the title compound (106 mmol, 73%). MS m/z=153 [M+H]+. Calculated for C7H8N2O2: 152.

後処理

  1. temperatureThe suspension was cooled in an ice-water bath
  2. concentrationThe reaction mixture was concentrated under reduced pressure
  3. customThe aqueous layer was separated
  4. extractionextracted with DCM (250 mL)
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated

出典と根拠

ORDレコード
ord-e733ce9f33084978a117ef350b278f75
出典データセット
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09296734B2

反応ノート

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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