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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210211Generated: November 2, 2026

Dichloromethane → HCID 15239200, compound

https://huagongshe.com/reaction/2210211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant3-Aminobenzoic AcidHCID 7419—
ReactantSodium BicarbonateHCID 516892—
Reactant3,4,4-Trifluoro-3-butenoyl chlorideHCID 10920789—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 15239200HCID 1523920069.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

2.2 g (0.0139 mole) 3,4,4-trifluoro-3-butenoyl chloride is added to a mixture of 3-aminobenzoic acid (1.37 g, 0.01 mole), sodium bicarbonate (0.84 g, 0.01 mole), water (20 mL) and dichloromethane (20 mL) with stirring at 0° C. After stirring for 15 min at room temperature, the mixture is diluted with ethyl acetate (100 mL) and water (50 mL). The organic layer is washed with 2N HCl and brine, and dried. The residue obtained after evaporation of the solvent is triturated with dry ether and filtered to give 1.8 g of the title compound as a light pink solid, a 69% yield. m.p. 252°-255° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05457134
Source datasetuspto-grants-1995_10
ORD IDord-b5115b9cb5914393b2b1280ee0faffdb
Source noteuspto-grants-1995_10