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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291422Generated: November 1, 2026

Nitric Acid → 1,3-Bis(2,6-dichloro-alpha,alpha,alpha-trifluoro-p-tolyloxy)-4-nitrobenzene

https://huagongshe.com/reaction/2291422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantSulfuric AcidHCID 1118—
Reactant1,3-Bis(2,6-dichloro-alpha,alpha,alpha-trifluoro-p-tolyloxy)-benzeneHCID 86735307—
Solvent1,2-DichloroethaneHCID 11—
Product1,3-Bis(2,6-dichloro-alpha,alpha,alpha-trifluoro-p-tolyloxy)-4-nitrobenzeneHCID 86735306—

Reaction Steps

A cooled mixture of concentrated sulfuric acid (6.5 ml.) and nitric acid (4.4 ml.) is added with stirring to an ice cold solution of 1,3-bis(2,6-dichloro-α,α,α-trifluoro-p-tolyloxy)-benzene (11.1 g. 0.021 mol) in 1,2-dichloroethane (30 ml.). After thirty minutes at room temperature, the phases are allowed to separate and the organic phase washed twice with water. Benzene (200 ml.) is added and the solution washed twice with dilute sodium carbonate solution, dried, filtered through activated silica gel (~25 g.), and the solvents removed. The residual crystals are triturated with pentane, filtered, and dried to obtain 1,3-bis(2,6-dichloro-α,α,α-trifluoro-p-tolyloxy)-4-nitrobenzene (9.9 g., 82%) m.p. 137.5°-140.5° C., 90% pure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04795825
Source datasetuspto-grants-1989_01
ORD IDord-fda9bc78eb9d443da54edaeafb48a689
Source noteuspto-grants-1989_01