2-Aminophenol → 2-Phenyl-3,4-dihydro-2H-1,4-benzoxazine

反応式

[O:1]1[C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=2[NH:4][CH2:3][CH2:2]1.N[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1O.ClC1C=CC=CC=1CC(Cl)=O>>[C:12]1([CH:2]2[CH2:3][NH:4][C:5]3[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=3[O:1]2)[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1

参加物

反応物 3

HCID 58012-Aminophenol

HCID 182669Acetyl chloride, 2-(2-chlorophenyl)-

HCID 5850963,4-Dihydro-2H-1,4-benzoxazine

生成物 1

HCID 137904912-Phenyl-3,4-dihydro-2H-1,4-benzoxazine

実験手順

By a procedure similar to that described for the synthesis of 3,4-dihydro-2H-1,4-benzoxazine (Example 142), o-aminophenol and 2-chlorophenylacetyl chloride produces 3,4-dihydro-2-phenyl-2H-1,4-benzoxazine, m.p. 113°-116° which, according to the reaction scheme of Example 110 is converted to the title compound, m.p. 311°-313°.

出典と根拠

ORDレコード: ord-c8f841f2896f4822ae83fc179f954723
出典データセット: uspto-grants-1977_03
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US04013652

反応ノート

読み込み中…

参加物