Chloroacetamide → methyl 9H-fluorene-9-carboxylate
反応式
Cl.CO.[Na].ClCC(N)=O.[CH3:10][O:11][C:12]([C:14]1(O)[C:26]2[CH:25]=[C:24](F)[CH:23]=[CH:22][C:21]=2[C:20]2[C:15]1=[CH:16][C:17](F)=[CH:18][CH:19]=2)=[O:13].[OH-].[Na+]>CO>[CH3:10][O:11][C:12]([CH:14]1[C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][C:20]=2[C:21]2[C:26]1=[CH:25][CH:24]=[CH:23][CH:22]=2)=[O:13]参加物
実験手順
9H-fluoren-9-carboxylic acid methyl ester (19), which was prepared by refluxing 9-Hfluoren-9-carboxylic acid (Aldrich Chemical, Inc.) in HCl/MeOH, (10.0 g, 44.6 mmol) was added to a solution of sodium (1.2 eq, 53.5 mmol, 1.23 g) in 100 mL methanol. After 15 min., 2-chloroacetamide (1.1 eq, 4.59 g) was added and the mixture was allowed to stir at room temperature under nitrogen for two (2) days. The reaction mixture was poured into 400 mL of cold 2.5% w/v aqueous sodium hydroxide and the insoluble material was removed by filtration. The filtrate was chilled and acidified with concentrated hydrochloric acid to precipitate the spiro-succinimide which was collected and air dried to provide 6.7 g (60%). Recrystallization from methanol gave purified (20), 4.28 g (39%). m.p. 237°-239° C. Calc. % C 77.09, % H 4.45, % N 5.62:meas. % C 77.17, % H 4.55, % N 5.58.
後処理
- additionThe reaction mixture was poured into 400 mL of cold 2.5%
- customthe insoluble material was removed by filtration
- temperatureThe filtrate was chilled
- customto precipitate the spiro-succinimide which
- customwas collected
- customair dried
- customto provide 6.7 g (60%)
- customRecrystallization from methanol
- customgave
- custompurified (20), 4.28 g (39%)
出典と根拠
- ORDレコード
- ord-c25d419af844430bb0c01ca680b1887d
- 出典データセット
- uspto-grants-1985_08
- 特許番号
- US04537892
反応ノート
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