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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2052734Generated: October 31, 2026

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

https://huagongshe.com/reaction/2052734

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 8673530682%

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° C., 90;l % pure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04185995
Source datasetuspto-grants-1980_01
ORD IDord-c5f940511f02410cbbfedc4acef3fb40
Source noteuspto-grants-1980_01