반응 #167190

ord-104096b1ab484dd39f16421339c64a7e

반응 방정식

COc1cc(C=O)ccc1O
4-hydroxy-3-methoxy-benzaldehyde
O=C([O-])[O-].[K+].[K+]
K2CO3
CC(=O)OCCBr
2-bromoethyl acetate
COc1cc(C=O)ccc1OCCOC(C)=O
title compound
수율 75.2%
COc1cc(C=O)ccc1OCCOC(C)=O
4-(2-acetoxy-ethoxy)-3-methoxy-benzaldehyde
수율 75.2%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도is refluxed for 48 h before it
  2. 2
    세척washed with water (2×200 mL)
  3. 3
    추출The washings are extracted with diethyl ether (200 mL)
  4. 4
    건조The combined organic extracts are dried over MgSO4
  5. 5
    농축concentrated
  6. 6
    기타The remaining residue is purified by column chromatography on silica gel eluting with heptane/EA 1:1

실험 절차

A mixture of 4-hydroxy-3-methoxy-benzaldehyde (2.5 g, 16.4 mmol), K2CO3 (6.81 g, 49.3 mmol) and 2-bromoethyl acetate (5.49 g, 32.9 mmol) in acetone (50 mL) is refluxed for 48 h before it is diluted with diethyl ether (250 mL) and washed with water (2×200 mL). The washings are extracted with diethyl ether (200 mL). The combined organic extracts are dried over MgSO4 and concentrated. The remaining residue is purified by column chromatography on silica gel eluting with heptane/EA 1:1 to afford the title compound (2.94 g) as colourless solid. 1H NMR (CDCl3): δ 9.85 (s, 1H), 7.45-7.41 (m, 2H), 6.99 (d, J=7.6 Hz, 1H), 4.51-4.47 (m, 2H), 4.34-4.30 (m, 2H), 3.94 (s, 3H), 2.11 (s, 3′-1).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: USRE045174E1uspto-grants-2014_09