반응 #595350

ord-2ea36c54df0948bda397cf370e38abdd

반응 방정식

Cl
hydrochloric acid
COCOCc1nc(-c2ccc(Cl)cc2)oc1C=O
compound
COCOCc1nc(-c2ccc(Cl)cc2)oc1C=O
2-(4-Chlorophenyl)-4-[(methoxymethoxy)methyl]-1,3-oxazole-5-carbaldehyde
C1COCCO1
dioxane
[Na+].[OH-]
sodium hydroxide
COCOCc1nc(-c2ccc(Cl)cc2)oc1C(=O)O
2-(4-Chlorophenyl)-4-[(methoxymethoxy)methyl]-1,3-oxazole-5-carboxylic acid

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    여과The mixture is then filtered through Celite, which
  2. 2
    세척is washed with warm water
  3. 3
    기타The filtrate obtained
  4. 4
    추출extracted three times with in each case 20 ml of diethyl ether
  5. 5
    건조The combined organic phases are dried over magnesium sulfate
  6. 6
    기타the solvent is removed on a rotary evaporator
  7. 7
    기타The residue is purified by preparative HPLC (column: YMC GEL ODS-AQ S-5/15 μm; mobile phase gradient: acetonitrile/water 10:90→95:5)

실험 절차

556 mg (2.25 mmol) of the compound from Example 41A and 14.7 ml of dioxane are added to a suspension of 802 mg (4.72 mmol) of silver(I) nitrate in 2 ml of water. A solution of 193 mg (4.84 mmol) of sodium hydroxide in 7.8 ml of water is then added slowly. The mixture is stirred at RT for 3 h. The mixture is then filtered through Celite, which is washed with warm water. The filtrate obtained is acidified by addition of 1 N hydrochloric acid and extracted three times with in each case 20 ml of diethyl ether. The combined organic phases are dried over magnesium sulfate and the solvent is removed on a rotary evaporator. The residue is purified by preparative HPLC (column: YMC GEL ODS-AQ S-5/15 μm; mobile phase gradient: acetonitrile/water 10:90→95:5).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09095582B2uspto-grants-2015_08