4-Isopropylaniline → (4-Isopropylphenyl)[4-(trifluoromethoxy)benzyl]amine

反応式

[F:1][C:2]([F:13])([F:12])[O:3][C:4]1[CH:11]=[CH:10][C:7]([CH:8]=O)=[CH:6][CH:5]=1.[CH:14]([C:17]1[CH:23]=[CH:22][C:20]([NH2:21])=[CH:19][CH:18]=1)([CH3:16])[CH3:15]>>[CH:14]([C:17]1[CH:23]=[CH:22][C:20]([NH:21][CH2:8][C:7]2[CH:10]=[CH:11][C:4]([O:3][C:2]([F:13])([F:12])[F:1])=[CH:5][CH:6]=2)=[CH:19][CH:18]=1)([CH3:16])[CH3:15]

参加物

反応物 2

HCID 74644-Isopropylaniline

HCID 69573p-(Trifluoromethoxy)benzaldehyde

生成物 1

HCID 59797515(4-Isopropylphenyl)[4-(trifluoromethoxy)benzyl]amine

実験手順

Following the procedure described in Example 1A, step 1, 4-(trifluoromethoxy)benzaldehyde and 4-isopropylaniline gave the title compound as a colorless oil.

出典と根拠

ORDレコード: ord-ce2ff44b7d8648bdae8a132a82ecdd80
出典データセット: uspto-grants-2008_09
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US07429666B2

反応ノート

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