반응 #82869

ord-25e19a8ecbfe48e2aab63a4bb4fc0483

반응 방정식

O=C([O-])[O-].[Cs+].[Cs+]
Cs2CO3
COc1ccc(C=O)cc1O
3-hydroxy-4-methoxybenzaldehyde
BrC1CCCC1
cyclopentyl bromide
BrC1CCCC1
cyclopentyl bromide
COc1ccc(C=O)cc1OC1CCCC1
title compound
수율 89.4%
COc1ccc(C=O)cc1OC1CCCC1
3-Cyclopentyloxy-4-methoxybenzaldehyde
수율 89.4%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    여과After a further 6h at RT, the mixture was filtered
  2. 2
    농축concentrated in vacuo
  3. 3
    workup.DISSOLUTIONThe residue was dissolved in CH2Cl2 (300 ml)
  4. 4
    세척washed with NaOH solution (10%, 2×150 ml)
  5. 5
    건조The organic layer was dried (MgSO4)
  6. 6
    농축concentrated in vacuo
  7. 7
    workup.DISTILLATIONdistilled (150° C., 10-2 mbar)

실험 절차

Cs2CO3 (214 g, 0.66 mol) was added to a mixture of 3-hydroxy-4-methoxybenzaldehyde (100 g, 0.66 mol) and cyclopentyl bromide (98 g, 0.66 mol) in anhydrous DMF (500 ml). The reaction mixture was stirred at RT for 16 h, then treated with a further portion of cyclopentyl bromide (98 g, 0.66 mol) and CS2CO3 (214 g, 0.66 mol). After a further 6h at RT, the mixture was filtered and concentrated in vacuo. The residue was dissolved in CH2Cl2 (300 ml) and washed with NaOH solution (10%, 2×150 ml). The organic layer was dried (MgSO4), concentrated in vacuo, and distilled (150° C., 10-2 mbar) to afford the title compound (130 g) as a viscous colorless oil. δH (CDCl3) 1.5-2.0 (8H, br m, CH2)4), 3.87 (3H, s, OCH3), 4.80 (1H, br m, OCHCH2), 6.90 (1H, d, J 8.7 Hz, ArH ortho to OMe), 7.30-7.45 (2H, m, 2×ArH meta to OMe), and 9.77 (1H, s, ArCHO).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05622977uspto-grants-1997_04