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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448033Generated: October 25, 2026

5-Fluoro-2-(trifluoromethyl)benzoyl chloride → HCID 69323879, compound

https://huagongshe.com/reaction/448033

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Fluoro-2-(trifluoromethyl)benzoyl chlorideHCID 2737560—
Reactant3-Butyl-2,4-dimethylthiazol-3-ium iodideHCID 69165109—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
SolventDimethyl sulfoxide methanolHCID 22036561—
ProductHCID 69323879HCID 69323879—

Reaction Steps

In a 20 mL vial a solution of 3-butyl-2,4-dimethylthiazol-3-ium iodide (47.92 mg, 0.16 mmol) dissolved in CH2Cl2 (0.5 mL) was added, followed by the addition of DMAP (49.24 mg, 0.40 mmol) dissolved in CH2Cl2 (0.8 mL). Then, to the solution was added 5-fluoro-2-(trifluoromethyl)benzoyl chloride (36.2 mg, 0.16 mmol) dissolved in CH2Cl2 (0.5 mL). The vial was capped and shaken overnight at room temperature. The residue was dissolved 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, MS and LC/MS. 1H NMR (500 MHz, DMSO-d6/D2O) δ ppm 0.90 (t, 3 H) 1.29-1.38 (m, 2H) 1.56-1.69 (m, 2 H) 2.28-2.32 (m, 3 H) 3.91-4.00 (m, 2 H) 6.00-6.05 (m, 1 H) 6.58-6.62 (m, 1 H) 7.37-7.45 (m, 2 H) 7.77-7.86 (m, 1 H); MS (ESI) positive ion 360 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481574B2
Source datasetuspto-grants-2013_07
ORD IDord-cf158add023d49bcbc3b85582b60203f
Source noteuspto-grants-2013_07