반응 #631996

ord-72dec71ed36a4d23a0be103cbf81a9ac

반응 방정식

C(=NC1CCCCC1)=NC1CCCCC1
DCC
C=Cc1ccc(C(=O)O)cc1
4-vinylbenzoic acid
CC(O)CC(=O)C1C(C)C=CCC1(C)C
3-hydroxy-1-(2,6,6-trimethyl-3-cyclohexen-1-yl)-1-butanone
C=Cc1ccc(C(=O)OC(C)CC(=O)C2C(C)C=CCC2(C)C)cc1
desired compound
수율 74.3%
C=Cc1ccc(C(=O)OC(C)CC(=O)C2C(C)C=CCC2(C)C)cc1
1-methyl-3-oxo-3-(2,6,6-trimethyl-3-cyclohexen-1-yl)propyl 4-vinylbenzoate
수율 74.3%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    여과The precipitate was filtered off
  2. 2
    세척washed twice with 10% aqueous HCl, saturated aqueous Na2CO3 and saturated aqueous NaCl
  3. 3
    건조The organic phases were dried over Na2SO4
  4. 4
    농축concentrated

실험 절차

A solution of DCC (3.60 g, 17.5 mmol) in 10 ml of CH2Cl2 was added to an ice-cold solution of 4-vinylbenzoic acid (2.35 g, 15.9 mmol), DMAP (1.55 g, 12.7 mmol) and 3-hydroxy-1-(2,6,6-trimethyl-3-cyclohexen-1-yl)-1-butanone (4.00 g, 19.1 mmol) in 30 ml of CH2Cl2. The reaction mixture was stirred at room temperature for 5 days. The precipitate was filtered off and the filtrate taken up in CH2Cl2, washed twice with 10% aqueous HCl, saturated aqueous Na2CO3 and saturated aqueous NaCl. The organic phases were dried over Na2SO4 and concentrated. Flash-chromatography over SiO2 (heptane/ether 9:1) gave 4.02 g of the desired compound (yield: 74%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07935669B2uspto-grants-2011_05