Tetrahydrofuran → HCID 19850253, 화합물

HRID 1252795

반응식

HRID 1252795 반응식
[CH3:1][C:2]1[O:6][C:5]2[CH2:7][CH2:8][CH2:9][C:10](=[O:11])[C:4]=2[CH:3]=1.[CH2:12]1COCC1>>[CH3:1][C:2]1[O:6][C:5]2[CH2:7][CH2:8][C:9](=[CH2:12])[C:10](=[O:11])[C:4]=2[CH:3]=1

참가 물질

3

반응물 2

HCID 8028TetrahydrofuranHCID 64216646,7-Dihydro-2-methyl-4(5H) benzofuranone

생성물 1

HCID 19850253HCID 19850253, 화합물

실험 절차

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-methylanilium trifluoroacetate (TAMA) (243 g) and trioxymethylene (99 g) over 31/2 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. customseparate portions, N-methylanilium trifluoroacetate (TAMA) (243 g) and trioxymethylene (99 g) over 31/2 hours
  2. temperaturethe mixture refluxed for 20 hours
  3. temperatureThe mixture was cooled
  4. custompartitioned between Et2O and water
  5. customthe layers separated
  6. extractionthe aqueous layer was extracted twice with Et2O
  7. washThe combined Et2O layers were washed exhaustively with water, with NaHCO3
  8. dry with materialwith brine, dried over MgSO4 and conc. in vacuo
  9. customto yield an amber oil
  10. customchromatographed on silica gel
  11. additionFractions containing the
  12. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-ad096d11a6324ecf8a705246a4472436
출처 데이터셋
uspto-grants-1988_05
특허 번호
US04745222

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