反応 #57070

ord-88e7ded5a61e46328892f889f67ed6cb

反応方程式

CCN(CC)CC.Cl
triethylamine hydrochloride
C1CCOC1
THF
CC(=O)[O-].[Na+]
sodium acetate
CC(=O)O[C@@H]1C=Cc2ccccc2[C@H]1O
2
CC(=O)O[C@@H]1C=Cc2ccccc2[C@H]1O
(1R*,2R*)-Acetic acid 1-hydroxy-1,2-dihydro-naphthalen-2-yl-ester

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他To a flame dried round bottom flask
  2. 2
    温度The mixture was heated
  3. 3
    温度at reflux for 3 hours
  4. 4
    その他the solvents were removed in vacuio
  5. 5
    その他The resulting mixture was purified by flash chromatography (30% ethyl acetate in hexanes)

実験手順

To a flame dried round bottom flask, [Rh(COD)Cl]2 (4.3 mg, 0.008 mmol DPPF (9.6 mg, 0.017 mmol),1 (50 mg, 1.39 mmol), and sodium acetate (142 mg, 1.74 mmol) were added followed by addition of THF (2 mL) and triethylamine hydrochloride (239 mg, 1.74 mmol). The mixture was heated at reflux for 3 hours and the solvents were removed in vacuio. The resulting mixture was purified by flash chromatography (30% ethyl acetate in hexanes) to give 2 as a crystalline solid (41 mg), 63%). Rf=0.26 on silica gel (20% ethyl acetate:hexanes); mp 67-68° (Et2O); IR (KBr, cm−1) 1H NMR (400 MHz, CDCl3) δ 7.54-7.53 (1H, m), 7.29-7.24 (2H, m), 7.10-7.08 (1H, m), 6.50 (1H, dd, J=3.9, 1.3 Hz), 5.85 (1H, dd, J=9.9, 3.1 Hz), 5.59 (1H, ddd, J=9.0, 2.8, 1.9 Hz), 4.92 (1H, d, J=9.0 Hz), 2.64 (1H, s), 2.12 (3H, s); 13C NMR (400 MHz, CDCl3) δ 171.3, 135.2, 131.5, 129.5, 128.3, 126.7, 126.0, 125.4, 75.3, 71.7, 21.2. HRMS calcd for C12H12O3 (M+): 204.0786. Found: 204.0791.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07420003B2uspto-grants-2008_09