反応式
C1C2CC3C(=CC=CC=3)C=2C=CC=1C(Cl)=O.CN.[CH3:19][NH:20][C:21]([C:23]1[CH:35]=[CH:34][C:33]2[C:32]3[C:27](=[CH:28][CH:29]=[CH:30][CH:31]=3)[CH2:26][C:25]=2[CH:24]=1)=O.[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1.CCOCC>[CH3:19][NH:20][CH2:21][C:23]1[CH:35]=[CH:34][C:33]2[C:32]3[C:27](=[CH:28][CH:29]=[CH:30][CH:31]=3)[CH2:26][C:25]=2[CH:24]=1参加物
7
実験手順
A solution of fluorene-2-carbonyl chloride (prepared from fluorene-2-carboxylic acid and oxalyl chloride) in THF is added to aqueous methylamine (2 molar equivalents) to prepare N-methyl fluorene-2-carboxamide. Reduction of the amide using LiAlH4 in ether provides 2-((methylamino)methyl)fluorene. The amine is protected by reaction with di-tert-butyl dicarbonate to provide 2-((N-tBOC-N-methylamino)methyl)fluorene.
出典と根拠
- ORDレコード
- ord-fed1647a2c5646559da749e107c1a7db
- 出典データセット
- uspto-grants-2015_02
- 特許番号
- US08946405B2
関連ノート
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