Chloroacetamide → methyl 9H-fluorene-9-carboxylate

HRID 485704ノート

反応式

HRID 485704 の反応式
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

7

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

  1. additionThe reaction mixture was poured into 400 mL of cold 2.5%
  2. customthe insoluble material was removed by filtration
  3. temperatureThe filtrate was chilled
  4. customto precipitate the spiro-succinimide which
  5. customwas collected
  6. customair dried
  7. customto provide 6.7 g (60%)
  8. customRecrystallization from methanol
  9. customgave
  10. 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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