반응 #411407

ord-7f7a5872e19d461387095ee136dc3a75

반응 방정식

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-naphthalenecarboxylate

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타for 30 minutes
  2. 2
    기타the reaction mixture partitioned between pentane (100 ml) and water (100 ml)
  3. 3
    추출The aqueous phase was extracted with pentane (100 ml)
  4. 4
    세척the combined organic layers washed with saturated aqueous NaCl (100 ml), dried MgSO4), and
  5. 5
    농축concentrated
  6. 6
    기타to yield an off-white solid
  7. 7
    기타Purification by flash chromatography (silica, 10% EtOAc-hexane)

실험 절차

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 Tefluxed 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).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06218128B1uspto-grants-2001_04