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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448085Generated: October 29, 2026

5-Chloro-2-fluorobenzoyl chloride → HCID 69188086, compound

https://huagongshe.com/reaction/448085

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-2-fluorobenzoyl chlorideHCID 2773604—
Reactant3-Butyl-2,4,5-trimethylthiazol-3-ium iodideHCID 69165591—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductHCID 69188086HCID 69188086—

Reaction Steps

In a 20 mL vial 3-butyl-2,4,5-trimethylthiazol-3-ium iodide (48 mg in 0.5 mL DMA, 0.16 mmol, 1 equiv.) was added, followed by TEA (38 mg in 0.5 mL DMA, 0.37 mmol, 2.4 equiv.) and the solution went black. DMAP (2 mg in 0.5 mL DMA, 0.016 mmol, 0.1 equiv) was added next, followed by 5-chloro-2-fluorobenzoyl chloride (0.9 mL of 0.2M in DMA, 1.2 equiv). The mixture was shaken overnight at room temperature and then concentrated in vacuo. The resulting residue was taken up in 1:1 DMSO/MeOH and purified by reverse phase HPLC using a method analogous to that described in Example 53 to provide the title compound. 1H NMR (500 MHz, DMSO-d6/D2O) δ ppm 0.93 (t, 3 H) 1.33-1.42 (m, 2 H) 1.61-1.68 (m, 2 H) 2.19 (s, 3 H) 2.23 (s, 3 H) 3.94-4.01 (m, 2 H) 6.36 (s, 1 H) 7.27-7.35 (m, 1 H) 7.47-7.53 (m, 1 H) 7.75-7.81 (m, 1H); MS (ESI) m/z 340 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481574B2
Source datasetuspto-grants-2013_07
ORD IDord-c13753b1ae19450483d1dda0067e234f
Source noteuspto-grants-2013_07