Water → HCID 19972408, compound
Reaction equation
[Na].[Cl:2][CH2:3][C:4]1[C:13]2[O:12][C:11]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)=[C:10]([CH3:20])[C:9](=[O:21])[C:8]=2[CH:7]=[CH:6][CH:5]=1.O.[O:23]1[CH2:28][CH2:27][O:26][CH2:25][CH2:24]1>C1(C)C(C)=CC=CC=1.C(O)CO>[Cl:2][CH2:3][C:4]1[C:13]2[O:12][C:11]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)=[C:10]([CH3:20])[C:9](=[O:21])[C:8]=2[CH:7]=[CH:6][CH:5]=1.[OH:23][CH2:28][CH2:27][O:26][CH2:25][C:24]1[C:13]2[O:12][C:11]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)=[C:10]([CH3:20])[C:9](=[O:21])[C:8]=2[CH:7]=[CH:6][CH:5]=1Participants
8
Procedure
A solution of 2.5 g of Intermediate XIX in 25 ml of xylene and 3 ml of dioxane was prepared. 0.15 g of sodium was dissolved in 3.10 ml of anhydrous ethylene glycol, and this solution was added dropwise at ambient temperature to the solution of Intermediate XIX. After refluxing for 5.5 hours, the reaction mixture was cooled to ambient temperature and poured into 50 ml of water. It was extracted with dichloromethane, and the extract was washed with sodium chloride solution, dried on anhydrous sodium sulfate and evaporated to dryness in vacuo. The solid residue was crystallized from ethanol, giving 2.1 g of the title compound, m.p. 132°-133° C.
Workup
- temperatureAfter refluxing for 5.5 hours
- extractionIt was extracted with dichloromethane
- washthe extract was washed with sodium chloride solution
- dry with materialdried on anhydrous sodium sulfate
- customevaporated to dryness in vacuo
- customThe solid residue was crystallized from ethanol
Sources & evidence
- ORD record
- ord-f5643f8003644328a1146f24f19ed8e2
- Source dataset
- uspto-grants-1995_04
- Patent number
- US05403842
Reaction notes
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