Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2308404Generated: October 30, 2026

Toluene → HCID 178471854, compound

https://huagongshe.com/reaction/2308404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantDimethylformamideHCID 6228—
ReactantThionyl ChlorideHCID 24386—
Reactant2,4-dibromo-3-(difluoromethoxy)benzoic AcidHCID 2782772—
ReactantEthyl 3,3-dimethylaminoacrylateHCID 85819813—
SolventWaterHCID 962—
SolventTriethylamineHCID 8471—
ProductHCID 178471854HCID 178471854—

Reaction Conditions

Temperature35 °C

Reaction Steps

To a mixture of 2.4-dibromo-3-(difluoromethoxy) benzoic acid (10 g) and thionyl chloride (4.38 gm) was added a mixture of toluene (15 ml) and N,N-dimethyl formamide (0.2 ml). The reaction mixture was heated slowly to reflux and stirred at reflux for about 2.5 hours. The reaction mixture was then cooled to 35° C. and added a solution of ethyl 3,3-dimethylaminoacrylate (4.13 gm), and triethylamine (3.79 gm) in toluene (20 ml) drop-wise during a period of about 1 hour maintaining a temperature of 35-40° C. After the addition was over, the reaction temperature was slowly increased to 60-65° C. and stirred the reaction mixture for about 24 hours. Cooled the reaction mixture to 30° C., added water (20 ml) and stirred for about 10 minutes. The organic layer was separated, cooled to about 5° C. and cyclopropylamine (1.82 gm) was added to it drop-wise maintaining temperature at 8-10° C. during a period of about 10 minutes. Stirred the reaction mixture for about 2 hours, solvent was removed under vacuum (˜80% of the original amount) and cooled the reaction mixture to about 20° C. The solid separated was filtered and dried to afford ethyl 3-cyclopropylamino-2-[2,4-dibromo-3(difluoromethoxy) benzoyl]-2-propenoate (10 gm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06835848B1
Source datasetuspto-grants-2004_12
ORD IDord-32743444dbb7494d8a9d104dd929ee87
Source noteuspto-grants-2004_12