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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367124Generated: October 30, 2026

1,1,2,2-Tetrachloroethane → HCID 44203047, compound

https://huagongshe.com/reaction/2367124

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1,2,2-TetrachloroethaneHCID 6591—
Reactant3,6-Difluorophthalic anhydrideHCID 513918—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventHydrochloric AcidHCID 313—
ProductHCID 44203047HCID 44203047148.3%

Reaction Steps

To a solution of 3,6-difluorophthalic anhydride (3.0 g, 16.00 mmol) in 1,1,2,2-tetrachloroethane (30 mL) chlorobenzene (2.0 mL, 18.00 mmol) was added followed by the addition of aluminum chloride (4.40 g, 33.00 mmol). The reaction mixture was stirred at room temperature for 120 minutes followed by the stirring at 60° C. for an additional 90 minutes. It was cooled to room temperature, poured into ice water (300 mL) and diluted with 1M aqueous hydrochloric acid. The aqueous slurry was extracted with ethyl acetate (300 mL) and the organic layer was washed with water (70 mL), brine (70 mL) and dried over anhydrous sodium sulfate. Filtration and concentration resulted in a crude product, which was crystallized from ethyl acetate by the addition of hexane. The product was collected by filtration and dried in vacuo to give 2-[(4-chlorophenyl)carbonyl]-3,6-difluorobenzoic acid (3.52 g, 73% yield). 1HMR (400 MHz, CD3OD): 7.77 (s, 1H), 7.75 (s, 1H), 7.53 (s, 1H), 7.51 (s, 1H), 7.53-7.34 (m, 2H). MS (EI) for C14H7ClF2O3: 281 (M−H2O).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697737B2
Source datasetuspto-grants-2014_04
ORD IDord-52532a0b2ef34bbdb3c81450b53f92ca
Source noteuspto-grants-2014_04