2-(Trifluoromethyl)aniline → HCID 58297518, compound

HRID 590921Notes

Reaction equation

[F:1][C:2]([F:11])([F:10])[C:3]1[CH:9]=[CH:8][CH:7]=[CH:6][C:4]=1[NH2:5].[F:12][C:13]([F:25])([F:24])[C:14]([F:23])([F:22])[C:15](I)([F:20])[C:16]([F:19])([F:18])[F:17]>>[F:17][C:16]([F:18])([F:19])[C:15]([F:20])([C:8]1[CH:7]=[CH:6][C:4]([NH2:5])=[C:3]([C:2]([F:10])([F:11])[F:1])[CH:9]=1)[C:14]([F:22])([F:23])[C:13]([F:25])([F:24])[F:12]

Participants

Reactant 2

HCID 69222-(Trifluoromethyl)aniline

HCID 27751652-Iodoperfluorobutane

Product 1

HCID 58297518HCID 58297518, compound

Procedure

According to the method of 1-1 of Example 1, a target compound was prepared from 2-(trifluoromethyl)aniline and nonafluoro-s-butyliodide under the light-shielding reaction condition.

Sources & evidence

ORD record: ord-6f17de58cd334bdd845a7694956dc952
Source dataset: uspto-grants-2016_01
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US09237745B2

Reaction notes

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