p-Fluoronitrobenzene → 1-Nitro-4-{[4-(trifluoromethyl)benzyl]oxy}benzene

HRID 1768141

Reaction equation

F[C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][CH:3]=1.[F:11][C:12]([F:22])([F:21])[C:13]1[CH:20]=[CH:19][C:16]([CH2:17][OH:18])=[CH:15][CH:14]=1>>[F:11][C:12]([F:21])([F:22])[C:13]1[CH:20]=[CH:19][C:16]([CH2:17][O:18][C:2]2[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][CH:3]=2)=[CH:15][CH:14]=1

Participants

Reactant 2

HCID 9590p-Fluoronitrobenzene

HCID 676844-(Trifluoromethyl)benzenemethanol

Product 1

HCID 27437921-Nitro-4-{[4-(trifluoromethyl)benzyl]oxy}benzeneYield 82%

Procedure

The title compound is prepared in analogy to Example 3a) from 4-fluoro-nitro-benzene and 4-trifluoromethyl-benzyl alcohol. Yield 82% of a slightly brown solid. Mp.=80.5–81.5° C.

Sources & evidence

ORD record: ord-1fe62b044657475fbc37f9dc94b1a179
Source dataset: uspto-grants-2007_06
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07235581B2

Linked notes

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