反応式
[C:1]1([C:7]2[N:8]=[C:9]([CH2:18][CH2:19][C:20]([OH:22])=[O:21])[O:10][C:11]=2[C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Na].O.O.[Cl-].[Ca+2:27].[Cl-]>O.[OH-].[Na+]>[Ca+2:27].[C:1]1([C:7]2[N:8]=[C:9]([CH2:18][CH2:19][C:20]([O-:22])=[O:21])[O:10][C:11]=2[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1.[C:1]1([C:7]2[N:8]=[C:9]([CH2:18][CH2:19][C:20]([O-:22])=[O:21])[O:10][C:11]=2[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1参加物
6
実験手順
β-(4,5-Diphenyloxazol-2-yl)propionic acid (oxaprozin) was converted to the sodium salt by stirring the acid (6 kg) in distilled water (60 kg) and 46-48% sodium hydroxide liquor (1.85 kg). A filtered solution of calcium chloride dihydrate B.P. (2.44 kg) in distilled water was added and the title compound precipitated as a white solid. This was collected on a vacuum filter and washed with distilled water until the filtrate was free from chloride. The product was dried in an air oven to give a yield of 6.7 kg (98% of theory) of the title compound as a tetrahydrate.
後処理
- customthe title compound precipitated as a white solid
- customThis was collected on a vacuum
- filtrationfilter
- washwashed with distilled water until the filtrate
- customThe product was dried in an air oven
出典と根拠
- ORDレコード
- ord-4189c16cdb4e4027b1c300b2c1f8dc83
- 出典データセット
- uspto-grants-1984_08
- 特許番号
- US04465838
関連ノート
読み込み中…