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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1730151Generated: October 26, 2026

N,N-Dimethylaniline → Carbonochloridic acid, 2,4,5-trichlorophenyl ester

https://huagongshe.com/reaction/1730151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantPhosgeneHCID 6371—
Reactant2,4,5-TrichlorophenolHCID 7271—
Reactanttert-Butyl 2,4,5-trichlorophenyl carbonateHCID 86887—
SolventTolueneHCID 1140—
ProductCarbonochloridic acid, 2,4,5-trichlorophenyl esterHCID 85650—

Reaction Steps

T-Butyl 2,4,5-trichlorophenyl carbonate is a known compound and one method for its preparation is described in an article by W. Broadbent, J. S. Morley and B. E. Stone in the Journal of the Chemical Society (C), 1967 pages 2632-2637. Briefly, in this method a solution of phosgene in toluene is treated with 2,4,5-trichlorophenol at -10° C, followed by addition of dimethylaniline at such a rate that the reaction temperature is maintained at 5°-10° C. The mixture is heated to 20°-24° C and maintained at this temperature for 12 hours. The mixture is cooled by addition of ice and the suspension filtered. From the organic layer in the filtrate, 2,4,5-trichlorophenyl chloroformate is isolated. A solution of the crude 2,4,5-trichlorophenyl chloroformate in methylene chloride is reacted with a solution of t-butanol and quinoline in methylene chloride. The reaction mixture is maintained at 20°-24° C for 12 hours. The mixture is cooled by addition of ice and the suspension is filtered. From the organic layer in the filtrate t-butyl 2,4,5-trichlorophenyl carbonate is isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03991205
Source datasetuspto-grants-1976_11
ORD IDord-589c17123a64483dbcd7f01b213a8180
Source noteuspto-grants-1976_11