Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27314Generated: October 25, 2026

Nitric Acid → 1,3-Bis(2-chloro-alpha,alpha,alpha-trifluoro-p-tolyloxy)-4-nitrobenzene

https://huagongshe.com/reaction/27314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantSulfuric AcidHCID 1118—
ReactantHexaneHCID 8058—
Reactant1,3-Bis(2-chloro-alpha,alpha,alpha-trifluoro-p-tolyloxy)benzeneHCID 86735305—
SolventBenzene--water (1/1)HCID 22272175—
Product1,3-Bis(2-chloro-alpha,alpha,alpha-trifluoro-p-tolyloxy)-4-nitrobenzeneHCID 86735304—

Reaction Steps

1,3-Bis(2-chloro-α,α,α-trifluoro-p-tolyloxy)benzene (12 g. 0.0255 mole) is added to a mixture of concentrated nitric acid (12 g.) and sulfuric acid (15 g.) at 5° C. The temperature is then allowed to rise to 25°-30° C. with manual stirring and mild ice bath cooling and after 10-20 minutes, the oil solidifies. The mixture is taken up in water/benzene (400 ml)/hexane (400 ml) and the organic phase is washed with water, dried, filtered through activated silica gel (~20 g.), and the solvents removed. The residue is recrystallized from isopropanol to give 1,3-bis(2-chloro-α,α,α-trifluoro-p-tolyloxy)-4-nitrobenzene, (7.4 g. 56%) m.p. 110°-111.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04220468
Source datasetuspto-grants-1980_09
ORD IDord-4ae9ad4c84a74ddb99cfef1f5ccc5ab8
Source noteuspto-grants-1980_09