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3-(Trifluoromethyl)aniline → HCID 20512399, compound

HRID 894599
Notes
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Reaction equation

HRID 894599 reaction equation
Cl[CH:2]([CH3:15])[CH2:3][NH:4][C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([C:11]([F:14])([F:13])[F:12])[CH:6]=1.[F:16][C:17]([F:26])([F:25])[C:18]1[CH:19]=[C:20]([CH:22]=[CH:23][CH:24]=1)[NH2:21]>>[F:12][C:11]([F:14])([F:13])[C:7]1[CH:6]=[C:5]([NH:4][CH2:3][CH:2]([NH:21][C:20]2[CH:22]=[CH:23][CH:24]=[C:18]([C:17]([F:16])([F:25])[F:26])[CH:19]=2)[CH3:15])[CH:10]=[CH:9][CH:8]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 73753-(Trifluoromethyl)anilineHCID 20512435HCID 20512435, compound

Product 1

HCID 20512399HCID 20512399, compoundYield 76.6%

Procedure

N-(β-chloropropyl)-3-trifluoromethyl-aniline is reacted with 3-trifluoromethylaniline as described in Example 16, point (c) to obtain 1,2-bis(3'-trifluoromethylphenyl-amino)propane with a yield of 76.6%. The dihydrochloride of this base melts at 116°-120° C.

Sources & evidence

ORD record
ord-474b3d04c5894499afc040e8c0a07c76
Source dataset
uspto-grants-1981_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04284642

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes