反応式
C[O:2][C:3]1[CH:19]=[CH:18][C:6]([O:7][C:8]2[CH:13]=[CH:12][C:11]([C:14]([F:17])([F:16])[F:15])=[CH:10][N:9]=2)=[CH:5][CH:4]=1.Cl.N1C=CC=CC=1>O.Cl>[OH:2][C:3]1[CH:19]=[CH:18][C:6]([O:7][C:8]2[CH:13]=[CH:12][C:11]([C:14]([F:17])([F:15])[F:16])=[CH:10][N:9]=2)=[CH:5][CH:4]=1参加物
5
実験手順
The product from (c) (1.7 g) and excess of pyridine hydrochloride were heated together for 8 hours at 180° C. The mixture was cooled, diluted with water and 2-molar hydrochloric acid, and extracted with ether. The extracts were dried and evaporated to yield an oil identified as the required hydroxy compound.
後処理
- temperatureThe mixture was cooled
- extractionextracted with ether
- customThe extracts were dried
- customevaporated
- customto yield an oil
出典と根拠
- ORDレコード
- ord-b2b93f581afd4ba08de951bf7d3c848f
- 出典データセット
- uspto-grants-1981_11
- 特許番号
- US04302242
関連ノート
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