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Methanol → HCID 12289779、化合物

HRID 1191186
ノート
印刷プレビュー

反応式

HRID 1191186 の反応式
[Br:1][C:2]1[O:6][C:5]([C:7]([O:9]C)=[O:8])=[CH:4][C:3]=1[C:11]([CH3:14])([CH3:13])[CH3:12].CO.O.[OH-].[Na+]>C1COCC1>[Br:1][C:2]1[O:6][C:5]([C:7]([OH:9])=[O:8])=[CH:4][C:3]=1[C:11]([CH3:14])([CH3:13])[CH3:12]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 887MethanolHCID 962WaterHCID 14798Sodium HydroxideHCID 67412486HCID 67412486、化合物

生成物 1

HCID 12289779HCID 12289779、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

A solution of methyl 5-bromo-4-tert-butyl-furan-2-carboxylate (1.45 g, 5.57 mmol, prepared as described in the previous step) in a mixture of THF (15 mL), MeOH (10 mL), and H2O (5 mL) was treated with 3 M aqueous NaOH solution (3.00 mL, 9.00 mmol) and the resulting mixture was stirred at room temperature for 16 h. The solvent was removed under reduced pressure and the residue was dissolved in H2O (60 mL) and extracted with Et2O (2×30 mL). The aqueous layer was acidified to pH˜2 using 2 M HCl. The precipitate was isolated by filtration, washed with H2O (20 mL), and air-dried to yield 5-bromo-4-tert-butyl-furan-2-carboxylic acid. The filtrate was extracted with EtOAc (3×20 mL) and the combined extracts were dried over MgSO4 and filtered. The solvent was removed under reduced pressure to yield a second crop of 5-bromo-4-tert-butyl-furan-2-carboxylic acid. 1H-NMR (400 MHz, CDCl3) δ: 7.25 (s, 1H), 1.35 (s, 9H).

後処理

  1. customThe solvent was removed under reduced pressure
  2. dissolutionthe residue was dissolved in H2O (60 mL)
  3. extractionextracted with Et2O (2×30 mL)
  4. customThe precipitate was isolated by filtration
  5. washwashed with H2O (20 mL)
  6. customair-dried

出典と根拠

ORDレコード
ord-9bc53827dcf440f28dfa05044770657f
出典データセット
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08680098B2

反応ノート

読み込み中…

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