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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448075Generated: October 29, 2026

4-Cyanobenzoyl chloride → HCID 69188706, compound

https://huagongshe.com/reaction/448075

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Cyanobenzoyl chlorideHCID 80172—
Reactant3-Butyl-2,4,5-trimethylthiazol-3-ium iodideHCID 69165591—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductHCID 69188706HCID 69188706—

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 4-cyanobenzoyl 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) 1.32-1.45 (m, 2 H) 1.60-1.68 (m, 2 H) 2.19 (s, 3 H) 2.23 (s, 3 H) 4.06-4.12 (m, 2 H) 6.67 (s, 1 H) 7.90 (d, 2 H) 8.10 (d, 2 H); MS (ESI) m/z 313 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481574B2
Source datasetuspto-grants-2013_07
ORD IDord-ef764c61bd174f28ae2481b5a089eb2d
Source noteuspto-grants-2013_07