Aniline → N-phenyl-2-naphthylamine

反応式

[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1OS(C(F)(F)F)(=O)=O.[NH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>>[C:20]1([NH:19][C:2]2[CH:3]=[CH:4][C:5]3[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=3)[CH:1]=2)[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1

参加物

反応物 2

HCID 6115Aniline

HCID 45463412-Naphthyl Trifluoromethanesulfonate

生成物 1

HCID 8679N-phenyl-2-naphthylamine収率 98%

実験手順

Using the general procedure for anilines with 66.8 mg (0.242 mmol) of 2-naphthyltriflate and 30.0 μl (0.329 mmol) of aniline yielded N-phenyl-2-naphthylamine as a white solid (52 mg, 98%), whose NMR spectra were identical to commercial material available from Aldrich.

出典と根拠

ORDレコード: ord-489806137a8342ce9f1301a10c07a026
出典データセット: uspto-grants-1998_10
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US05817877

反応ノート

読み込み中…