反応式
[C:1](OCC)(=[O:7])[C:2](OCC)=[O:3].[CH2:11]([O:13][C:14](=[O:21])[CH2:15][S:16][CH2:17][C:18]([O-:20])=[O:19])[CH3:12].O.Cl.[CH3:24][CH2:25]O>>[C:18]([C:17]1[S:16][C:15]([C:14]([O:13][CH2:11][CH3:12])=[O:21])=[C:1]([OH:7])[C:2]=1[OH:3])([O:20][CH2:24][CH3:25])=[O:19]参加物
6
実験手順
Diethyl oxalate (6.58 g. 45 mmol) was added to 2.2° thiobisacetate ethyl ester (4.66 g. 23 mmol) to produce a yellow-orange solution. A solution of Na (1.56 g, 68 mmol) in EtOH (24 mL) was added to produce a white/yellow precipitate, this was mixed well for 10 minutes. H2O (50 mL) was added to the reaction mass with cooling in an ice bath. Concentrated HCl was added dropwise until acidified. This was allowed to stand in the refrigerator for 12 days. At this point a cold filtration was done to isolate a white solid.
後処理
- customto produce a yellow-orange solution
- customto produce a white/yellow precipitate
- additionthis was mixed well for 10 minutes
- temperaturewith cooling in an ice bath
- filtrationAt this point a cold filtration
- customto isolate a white solid
出典と根拠
- ORDレコード
- ord-51a03ac9c6464e8e91808ce3614aae87
- 出典データセット
- uspto-grants-2005_03
- 特許番号
- US06869729B1
関連ノート
読み込み中…