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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448084Generated: October 29, 2026

5-Fluoro-2-methylbenzoyl chloride → HCID 69188065, compound

https://huagongshe.com/reaction/448084

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Fluoro-2-methylbenzoyl chlorideHCID 2737383—
Reactant3-Butyl-2,4,5-trimethylthiazol-3-ium iodideHCID 69165591—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductHCID 69188065HCID 69188065—

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-fluoro-2-methylbenzoyl 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 0.91 (t, 3 H) 1.30-1.41 (m, 2 H) 1.55-1.68 (m, 2 H) 2.20 (s, 3 H) 2.22 (s, 3 H) 2.33 (s, 3 H) 3.96-4.04 (m, 2 H) 6.09 (s, 1 H) 7.08-7.14 (m, 1 H) 7.19-7.27 (m, 2 H); MS (ESI) m/z 320 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481574B2
Source datasetuspto-grants-2013_07
ORD IDord-6d99893b04794dc892e89e05f8b5b019
Source noteuspto-grants-2013_07