Sulfuric Acid → HCID 19850253, 화합물

HRID 1608050

반응식

HRID 1608050 반응식
OS(O)(=O)=O.O[C:7]1[CH2:12][CH2:11][CH2:10][C:9](=[O:13])[C:8]=1[CH2:14][C:15](=[O:17])[CH3:16].[CH2:18](Cl)Cl.O1C=CCC1=O>C1COCC1>[CH3:16][C:15]1[O:17][C:7]2[CH2:12][CH2:11][C:10](=[CH2:18])[C:9](=[O:13])[C:8]=2[CH:14]=1

참가 물질

6

반응물 4

HCID 1118Sulfuric AcidHCID 6344DichloromethaneHCID 1407652(3H)-FuranoneHCID 74817023-Hydroxy-2-(2-oxopropyl)-2-cyclohexen-1-one

생성물 1

HCID 19850253HCID 19850253, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of conc. H2SO4 (300 ml) cooled in an ice-bath was added a solution of 3-hydroxy-2-(2-oxopropyl)-2-cyclohexen-1-one (190 g in 300 ml CH2Cl2). Upon completion of addition, the mixture was stirred at ambient temperature for about 1 hour. The mixture was then slowly poured into 3 liters ice water, and then about 1 liter of CH2Cl2 was added. The layers are separated and the aqueous layer extracted thrice with CH2Cl2 and the combined CH2Cl2 layers again extracted thrice with water. The CH2Cl2 layer was washed thrice with dilute aqueous NaHCo3, then once with water and dried (MgSO4). Concentration in vacuo afforded an orange oil. Step B. To a solution of the furanone of Step A (164.5 g, 1.10 mole) in about 400 ml THF was added, in four separate portions, N-methylanilinium trifluoroacetate (TAMA) (243 g) and trioxymethylene (99 g) over 3-1/2 hours, and the mixture refluxed for 20 hours. The mixture was cooled and partitioned between Et2O and water, the layers separated and the aqueous layer was extracted twice with Et2O. The combined Et2O layers were washed exhaustively with water, with NaHCO3 and then with brine, dried over MgSO4 and conc. in vacuo to yield an amber oil. This oil was flash chromatographed on silica gel using CH2Cl2 as solvent in several runs of 10-20 g per run. Fractions containing the fast moving material were combined, concentrated in vacuo to obtain the desired product as a yellow oil.

후처리

  1. additionUpon completion of addition
  2. customThe layers are separated
  3. extractionthe aqueous layer extracted thrice with CH2Cl2
  4. washThe CH2Cl2 layer was washed thrice with dilute aqueous NaHCo3
  5. dry with materialonce with water and dried (MgSO4)
  6. concentrationConcentration in vacuo
  7. customafforded an orange oil
  8. customseparate portions, N-methylanilinium trifluoroacetate (TAMA) (243 g) and trioxymethylene (99 g) over 3-1/2 hours
  9. temperaturethe mixture refluxed for 20 hours
  10. temperatureThe mixture was cooled
  11. custompartitioned between Et2O and water
  12. customthe layers separated
  13. extractionthe aqueous layer was extracted twice with Et2O
  14. washThe combined Et2O layers were washed exhaustively with water, with NaHCO3
  15. dry with materialwith brine, dried over MgSO4 and conc. in vacuo
  16. customto yield an amber oil
  17. customchromatographed on silica gel
  18. additionFractions containing the
  19. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-8451ea1380674223b53793c6c730392c
출처 데이터셋
uspto-grants-1989_09
특허 번호
US04868315

연결된 노트

불러오는 중…