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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1467797Generated: October 26, 2026

1,2-Dibromo-1,1,2,2-tetrachloroethane → 2-Bromo-4-chloro-3-fluorobenzoic acid

https://huagongshe.com/reaction/1467797

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-Dibromo-1,1,2,2-tetrachloroethaneHCID 69426—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Chloro-3-fluorobenzoic acidHCID 2736536—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-Bromo-4-chloro-3-fluorobenzoic acidHCID 2330314983.3%

Reaction Conditions

Temperature-30 °C

Reaction Steps

To a cooled (−78° C.) solution of DIEA (4.9 mL, 48 mmol) in THF was added dropwise n-BuLi (132 mL, 2.3 eq, 2.5 M). The mixture was stirred at −30° C. for 30 min. Again the reaction mixture was cooled to −78° C., and a solution of 4-chloro-3-fluorobenzoic acid (25 g, 143 mmol) in THF was added over 1 h. The reaction was stirred at −78° C. overnight. The next day a solution of 1,2-dibromo-1,1,2,2-tetrachloroethane (87 g, 267 mmol) in THF was added and the reaction was stirred at −78° C. for further 2 h and then rt for 4 h. The reaction mixture was quenched with H2O, organic layer was separated and aqueous layer washed with Et2O. Aqueous layer acidified with 1.5 N HCl and extracted in EtOAc (2×200 mL), dried over anhydrous Na2SO4, filtered and concentrated to afford Intermediate 12A (30 g, 83.3%). MS (ESI) m/z: 252.6 (M−H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000172B2
Source datasetuspto-grants-2015_04
ORD IDord-db27bbdce64a4aafb301e5225d7cedfd
Source noteuspto-grants-2015_04