Hydrochloric Acid → 2,3-Dihydro-1-benzofuran-6-carboxylic acid
反応式
C(N(CCCC)CCCC)CCC.[C]=O.C[O:17][C:18]([C:20]1[CH:28]=[CH:27][C:23]2[CH2:24][CH2:25][O:26][C:22]=2[CH:21]=1)=[O:19].Cl>[Br-].[Br-].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[Pd+2].[OH-].[Na+]>[O:26]1[C:22]2[CH:21]=[C:20]([C:18]([OH:19])=[O:17])[CH:28]=[CH:27][C:23]=2[CH2:24][CH2:25]1参加物
反応条件
- 温度
- 100 °C
実験手順
Palladium bis(triphenylphosphine) dibromide (3 g) was added to a degassed methanolic solution (30 ml) of trifluoro-methanesulfonic acid 2,3-dihydro benzofuran-6-yl ester (5 g) and tributylamine (5 ml). The mixture was charged with carbon monoxide at 40 psi in a Berghoff pressure vessel then heated at 100° C. for 72 hours. The resulting methanolic solution of 2,3-dihydro-benzofuran-6-carboxylic acid methyl ester was treated with sodium hydroxide solution (50 ml of 2M aqueous solution) and stirred at room temperature for 18 hours. The reaction mixture was acidified to pH 1 with hydrochloric acid (5M aqueous solution) and extracted with ethyl acetate (300 ml). The ethyl acetate layer was separated and the product extracted into saturated sodium bicarbonate solution (200 ml). The sodium bicarbonate solution was acidified to pH 1 with hydrochloric acid (5M aqueous solution) and the resulting precipitate dissolved in ethyl acetate. The ethyl acetate layer was separated, dried (MgSO4) and evaporated to dryness under reduced pressure to yield the title compound (0.6 g, 20%). 1H NMR (250 MHz, CD3OD) δ: 3.20 (2H, t, J=8.6 Hz), 4.54 (2H, t, J=8.6 Hz), 7.23 (1H, d, J=8 Hz), 7.25 (1H, brs), 7.49(1H, dd, J=8 and 1 Hz).
後処理
- extractionextracted with ethyl acetate (300 ml)
- customThe ethyl acetate layer was separated
- extractionthe product extracted into saturated sodium bicarbonate solution (200 ml)
- dissolutionthe resulting precipitate dissolved in ethyl acetate
- customThe ethyl acetate layer was separated
- dry with materialdried (MgSO4)
- customevaporated to dryness under reduced pressure
出典と根拠
- ORDレコード
- ord-dce3e73df66f40a2b59c797a5805b2f8
- 出典データセット
- uspto-grants-2002_10
- 特許番号
- US06465493B1
反応ノート
読み込み中…