HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Fluoronitrobenzene → 1-Nitro-4-{[4-(trifluoromethyl)benzyl]oxy}benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | 4-(Trifluoromethyl)benzenemethanol | HCID 67684 | — |
| Product | 1-Nitro-4-{[4-(trifluoromethyl)benzyl]oxy}benzene | HCID 2743792 | 82% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07235581B2 |
| Source dataset | uspto-grants-2007_06 |
| ORD ID | ord-1fe62b044657475fbc37f9dc94b1a179 |
| Source note | uspto-grants-2007_06 |