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Methanol → Methyl 3-bromo-2-methoxybenzoate

HRID 561249
ノート
印刷プレビュー

反応式

HRID 561249 の反応式
S(=O)(=O)(O)O.[Br:6][C:7]1[C:8]([O:16][CH3:17])=[C:9]([CH:13]=[CH:14][CH:15]=1)[C:10]([OH:12])=[O:11].[CH3:18]O>>[CH3:18][O:11][C:10](=[O:12])[C:9]1[CH:13]=[CH:14][CH:15]=[C:7]([Br:6])[C:8]=1[O:16][CH3:17]
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 2535983-Bromo-2-methoxybenzoic acid

生成物 1

HCID 46311082Methyl 3-bromo-2-methoxybenzoate

実験手順

5.0 mL of sulfuric acid (H2SO4) was slowly added to a solution of 5.0 g of 3-bromo-2-methoxy-benzoic acid 4 in 100 mL of methanol (MeOH). The resulting solution was heated to reflux overnight. The solution was cooled to room temperature and quenched with sodium bicarbonate to pH 7. The aqueous layer was extracted several times with ethyl acetate. The combined organic extracts were washed with brine and dried over sodium sulphate. The resulting mixture was filtered. The solvents were evaporated under reduced pressure to afford 5.3 g of 3-bromo-2-methoxy-benzoic acid methyl ester 5.

後処理

  1. temperatureThe resulting solution was heated
  2. temperatureto reflux overnight
  3. customquenched with sodium bicarbonate to pH 7
  4. extractionThe aqueous layer was extracted several times with ethyl acetate
  5. washThe combined organic extracts were washed with brine
  6. dry with materialdried over sodium sulphate
  7. filtrationThe resulting mixture was filtered
  8. customThe solvents were evaporated under reduced pressure

出典と根拠

ORDレコード
ord-f4cdaf5cc87c4caa81a700effa703e63
出典データセット
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08063231B2

反応ノート

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