Water → HCID 20386919、化合物
反応式
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]1参加物
7
実験手順
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.
後処理
- temperatureThe solution was cooled
- filtrationfiltered with suction
- customto remove the precipitate
- customthe filtrate was evaporated to dryness at 0.1 mm Hg
- dissolutionThe residue was dissolved in ether
- washwashed with H2O
- dry with materialdried over MgSO4
- customthe solvent was removed by distillation under reduced pressure
- customThe oily residue which was not further purified
出典と根拠
- ORDレコード
- ord-50929daee64e4b7abec7201f16981ec6
- 出典データセット
- uspto-grants-1979_11
- 特許番号
- US04174458
反応ノート
読み込み中…