Boron tribromide → Methyl (5-hydroxy-2,3-dihydro-1H-inden-1-yl)acetate

HRID 1821055ノート

反応式

HRID 1821055 の反応式
B(Br)(Br)Br.C[O:6][C:7]1[CH:8]=[C:9]2[C:13](=[CH:14][CH:15]=1)[CH:12]([CH2:16][C:17]([O:19][CH3:20])=[O:18])[CH2:11][CH2:10]2>ClCCl>[OH:6][C:7]1[CH:8]=[C:9]2[C:13](=[CH:14][CH:15]=1)[CH:12]([CH2:16][C:17]([O:19][CH3:20])=[O:18])[CH2:11][CH2:10]2

参加物

4

反応物 2

HCID 25134Boron tribromideHCID 71710973Methyl (5-methoxy-2,3-dihydro-1H-inden-1-yl)acetate

生成物 1

HCID 53438903Methyl (5-hydroxy-2,3-dihydro-1H-inden-1-yl)acetate収率 92.9%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

A 1.0 M solution of boron tribromide in dichloromethane (22.7 mL, 22.7 mmol) was added to an ice-cold solution of methyl (R/S)-(5-methoxy-indan-1-yl)acetate (2.00 g, 9.08 mmol, from Step B) in dichloromethane (15 mL). The cooling bath was removed and the reaction mixture stirred at ambient temperature. After 1 hr, the reaction mixture was slowly transferred to an ice-cold solution of methanol (50 mL). Methanol was removed in vacuo, and the residue was partitioned between EtOAc and sat. NaH2PO4. The organic layer was washed with H2O, brine, and dried over MgSO4. The mixture was filtered, concentrated in vacuo and purified by flash chromatography (15, 20% EtOAc/hexanes) on SiO2 to afford 1.74 g of the title compound: 1H NMR (CDCl3) δ 1.72-1.79 (m, 1H), 2.35-2.42 (m, 1H), 2.46 (dd, 1H, J=8.5, 15.3 Hz), 2.76 (dd, 1H, J=5.9, 15.3 Hz), 2.80-2.92 (m, 2H), 3.50-3.55 (m, 1H), 3.75 (s, 3H), 5.63-5.86 (brs, 1H), 6.67 (dd, 1H, J=2.4, 8.1 Hz), 6.74 (d, 1H, J=2.0 Hz), 7.01 (d, 1H, J=8.3 Hz).

後処理

  1. customThe cooling bath was removed
  2. customMethanol was removed in vacuo
  3. customthe residue was partitioned between EtOAc and sat. NaH2PO4
  4. washThe organic layer was washed with H2O, brine
  5. dry with materialdried over MgSO4
  6. filtrationThe mixture was filtered
  7. concentrationconcentrated in vacuo
  8. custompurified by flash chromatography (15, 20% EtOAc/hexanes) on SiO2

出典と根拠

ORDレコード
ord-db5dc891434b488083bd335aeadd3e7f
出典データセット
uspto-grants-2009_10
特許番号
US07605171B2

反応ノート

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