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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1074847Generated: October 26, 2026

Ammonia → Aclonifen

https://huagongshe.com/reaction/1074847

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantPhenolHCID 996—
ReactantSodium HydroxideHCID 14798—
Reactant2,3,4-TrichloronitrobenzeneHCID 28697—
SolventAcetic AcidHCID 176—
SolventDimethyl SulfoxideHCID 679—
ProductAclonifenHCID 92389—

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 911 gm (4 mole) of 2,3,4-trichloronitrobenzene was dissolved in 4 liters of dimethyl sulfoxide and mixed in a 10-liter autoclave with 400 ml of liquid ammonia. The autoclave was closed and kept at 50° C. for 24 hours, a pressure of 5.3 bars being set. After cooling of the mixture and ventilation of the pressure vessel, the mixture was removed and stirred in a 15 liter vessel with 400 gm of 40% (% by weight) sodium hydroxide solution. In so doing, ammonia escaped and was drawn off. Four hundred sixteen grams of phenol (4.4 mol) were then added to the solution which was heated to 50° C., and 440 gm of 40% by weight solution of sodium hydroxide solution were dropped therein. The mixture was stirred for 7 hours at 50°-60° C. To complete the reaction, 41 gm of phenol and 44 gm of 40% by weight solution of sodium hydroxide were added again, and the mixture was kept at 60° C. for a further 3 hours. The mixture was allowed to cool and was acidified with 100 ml of glacial acetic acid, and the product was precipitated with ice water by trituration. The yellowy brown solid crude product was extracted, washed with water, and dried. The crude product (980 gm m.p. 70°-78° C.) was recrystallized from 2.5 liters of isopropanol. The yield was 800 gm (75.5% of theory) of a yellowy brown solid, m.p. 81.5°-83.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04394159
Source datasetuspto-grants-1983_07
ORD IDord-e3443f7db6484cdb8075926be07562c3
Source noteuspto-grants-1983_07