反应 #705239

ord-429bbd76cd2347c6b4fdaa39371689c7

反应方程式

O=C(O)c1ccc2cc(Br)ccc2c1
6-bromo-2-naphthalenecarboxylic acid
O=C(O)c1ccc2cc(Br)ccc2c1
Compound M
O=C(O)c1ccc2cc(Br)ccc2c1
6-bromo-2-naphthalenecarboxylic acid
CCO
ethanol
O=S(=O)(O)O
sulfuric acid
CCOC(=O)c1ccc2cc(Br)ccc2c1
title compound
CCOC(=O)c1ccc2cc(Br)ccc2c1
Ethyl 6-bromo-2-naphthalene carboxylate

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度The solution was refluxed for 30 minutes
  2. 2
    其他the reaction mixture partitioned between pentane (100 ml) and water (100 ml)
  3. 3
    萃取The aqueous phase was extracted with pentane (100 ml)
  4. 4
    洗涤the combined organic layers washed with saturated aqueous NaCl (100 ml)
  5. 5
    干燥dried (MgSO4)
  6. 6
    浓缩concentrated
  7. 7
    其他to yield an off-white solid
  8. 8
    其他Purification by flash.chromatography (silica, 10% EtOAc-hexane)

实验过程

To a solution of 6-bromo-2-naphthalenecarboxylic acid (Compound M) 3.1 g, (12.43 mmol) in ethanol (30 ml, 23.55 g, 511.0 mmol) was added 18M sulfuric acid (2 ml). The solution was refluxed for 30 minutes, cooled to room temperature, and the reaction mixture partitioned between pentane (100 ml) and water (100 ml). The aqueous phase was extracted with pentane (100 ml) and the combined organic layers washed with saturated aqueous NaCl (100 ml), dried (MgSO4), and concentrated to yield an off-white solid. Purification by flash.chromatography (silica, 10% EtOAc-hexane) afforded the title compound as a white solid. 1H NMR (CDCl3): δ 8.58 (1H, br s), 8.10 (1H, dd, J=1.7, 9 Hz), 8.06 (1H, d, J=2 Hz), 7.83 (1H, d, J=9 Hz), 7.80 (1H, d, J=9 Hz), 7.62 (1H, dd, J=2, 9 Hz).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05952345uspto-grants-1999_09