반응 #1014

ord-8d66976050a242adaad6949712ee0b51

반응 방정식

O=C([O-])[O-].[Cs+].[Cs+]
Caesium carbonate
COc1ccc(C=O)cc1O
3-hydroxy-4-methoxybenzaldehyde
BrC1CCCC1
cyclopentyl bromide
BrC1CCCC1
cyclopentyl bromide
O=C([O-])[O-].[Cs+].[Cs+]
caesium carbonate
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
    workup.WAITAfter a further 6 h at RT
  2. 2
    여과the mixture was filtered
  3. 3
    농축concentrated in vacuo
  4. 4
    workup.DISSOLUTIONThe residue was dissolved in dichloromethane (300 ml)
  5. 5
    세척washed with sodium hydroxide solution (10%; 2×150 ml)
  6. 6
    건조The organic layer was dried (MgSO4)
  7. 7
    농축concentrated in vacuo
  8. 8
    workup.DISTILLATIONdistilled (150° C., 10-2 mbar)

실험 절차

Caesium carbonate (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 (50 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 caesium carbonate (214 g, 0.66 mol). After a further 6 h at RT, the mixture was filtered and concentrated in vacuo. The residue was dissolved in dichloromethane (300 ml) and washed with sodium hydroxide 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 colourless oil. (Found: C, 70.38; H, 7.48. C13H16O3 requires C, 70.89; H 7.32%); δH (CDCl3) 1.5-2.0 (8H, br m, CH2)4), 3.87 (3H, s, OMe), 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 (1 H, s, ArCHO).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05723460uspto-grants-1998_03