Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 321994Generated: October 26, 2026

Carbon Dioxide → 2,3-Dichloro-6-iodobenzoic acid

https://huagongshe.com/reaction/321994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantDiisopropylamineHCID 7912—
ReactantBenzene, 1,2-dichloro-4-iodo-HCID 88591—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2,3-Dichloro-6-iodobenzoic acidHCID 22008816—

Reaction Conditions

Temperature-78 °C

Reaction Steps

n-Butyllithium (1.45M solution in hexane, 19.4 mmol, 13.4 ml) was added dropwise to a stirred solution of diisopropylamine (21.4 mmol, 3.0 ml) in THF (90 ml) at 0° C. After 30 minutes, the solution was cooled to −78° C. and a solution of 1,2-dichloro-4-iodobenzene (5.30 g, 19.4 mmol) in TIF (10 ml) was added dropwise. After 10 minutes, solid carbon dioxide was added cautiously and the allowed to warm to room temperature over 16 h. The mixture was diluted with water and extracted twice with ethyl acetate. The aqueous layer was acidified with dilute aqueous hydrochloric acid and then extracted twice with ethyl acetate. The extracts were dried over sodium sulphate and evaporated to give the title compound as a yellow solid (3.59 g). 300 MHz 1H NMR (d6-DMSO) 11.5 (1H, br.s), 7.82 (1H, d, J 8.4 Hz), 7.44 (1H, d, J 8.4 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211189B1
Source datasetuspto-grants-2001_04
ORD IDord-c0a86ed9408c4d2a90ae053d191ec308
Source noteuspto-grants-2001_04