Water → HCID 20386919, 화합물

HRID 46708노트

반응식

HRID 46708 반응식
S1CCS[CH:2]1[CH:6]1[CH:17](/[CH:18]=[CH:19]/[CH:20]([OH:26])[CH2:21][CH2:22][CH2:23][CH2:24][CH3:25])[CH2:16][CH2:15][C:7]21[O:12][CH2:11][C:10]([CH3:14])([CH3:13])[CH2:9]O2.[O:27]1[CH2:32][CH2:31][CH2:30][CH2:29][CH:28]1OC1CCCCO1.CI.[C:42]([O-:45])([O-])=O.[Ca+2].[OH2:47].[CH3:48]N(C=O)C>CC(C)=O>[CH3:14][C:10]1([CH3:9])[CH2:11][O:12][C:7]2([CH2:15][CH2:16][CH:17](/[CH:18]=[CH:19]/[CH:20]([CH2:21][CH2:22][CH2:23][CH2:24][CH3:25])[O:26][CH:28]3[CH2:29][CH2:30][CH2:31][CH2:32][O:27]3)[CH:6]2[CH2:2][CH2:48][CH:42]=[O:45])[O:47][CH2:13]1

참가 물질

7

실험 절차

1.05 g [2.05 mmoles] of 1[7-[(1,3-dithia-2-cyclopentyl)]-3,3-dimethyl-1,5-dioxaspiro[5,4]-dec-8-yl]-trans-1-octene-3-ol-tetrahydropyranyl ether was stirred for 2 hours at 50° C. in 100 ml of DMF with 0.7 ml (10.3 mmoles) of methyl iodide, 1.4 g (14 moles) of CaCO3 and 0.4 ml of H2O. The solution was cooled, combined with 50 ml of acetone, filtered with suction to remove the precipitate and the filtrate was evaporated to dryness at 0.1 mm Hg. The residue was dissolved in ether, washed with H2O, dried over MgSO4 and the solvent was removed by distillation under reduced pressure. The oily residue which was not further purified showed in the infrared spectrum a strong carbonyl band at 1730 cm-1.

후처리

  1. temperatureThe solution was cooled
  2. filtrationfiltered with suction
  3. customto remove the precipitate
  4. customthe filtrate was evaporated to dryness at 0.1 mm Hg
  5. dissolutionThe residue was dissolved in ether
  6. washwashed with H2O
  7. dry with materialdried over MgSO4
  8. customthe solvent was removed by distillation under reduced pressure
  9. customThe oily residue which was not further purified

출처 및 근거

ORD 기록
ord-50929daee64e4b7abec7201f16981ec6
출처 데이터셋
uspto-grants-1979_11
특허 번호
US04174458

반응 노트

불러오는 중…