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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354313Generated: October 28, 2026

Trifluoroacetic acid → Ethyl 2-(3,4-dichloroanilino)acetate

https://huagongshe.com/reaction/2354313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant3,4-DichloroanilineHCID 7257—
ReactantEthyl bromoacetateHCID 7748—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
SolventAcetonitrile--water (1/1)HCID 18373917—
ProductEthyl 2-(3,4-dichloroanilino)acetateHCID 272780497%

Reaction Steps

3,4-Dichloroaniline (100 g, 0.617 mol), ethyl bromoacetate (68.4 mL, 0.617 mol), and diisopropylethylamine (129.0 mL, 0.740 mol) were combined in 300 mL of dry NMP and stirred at room temperature for 18 h. HPLC (Eclipse XDB-C18, 4.6×250 mm, 5 micron, 1-99% CH3CN/H2O with 0.1% trifluoroacetic acid) after 18 h at room temperature showed that most of the starting material (Rt=5.2 min) was consumed and that a new peak had formed (Rt=7.9 min). The reaction was heated to 90° C. for 1 h, at which point HPLC indicated that conversion was complete. The reaction was allowed to cool to room temperature and then poured onto 2.5 L of ice, 1.5 L of water, and 240 g of NaHCO3. A tan precipitate formed immediately, the suspension was stirred vigorously for 10 minutes and then filtered through a fritted glass funnel. The tan solid was air-dried for 20 h in a crystallizing dish and then transferred to a 1 L flask and dried by rotary evaporation to remove the bulk of the remaining water. The tan solid was further dried under high vacuum to give 148 g (97%) of the title compound. LC/MS (APCI) m/e 248 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07749998B2
Source datasetuspto-grants-2010_07
ORD IDord-d7d96c53b30d423eb1db0dff444874bd
Source noteuspto-grants-2010_07