HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448077Generated: October 30, 2026
2,5-Difluorobenzoyl chloride → HCID 69324490, compound
https://huagongshe.com/reaction/448077
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,5-Difluorobenzoyl chloride | HCID 588082 | — |
| Reactant | 3-Butyl-2,4,5-trimethylthiazol-3-ium iodide | HCID 69165591 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Product | HCID 69324490 | HCID 69324490 | — |
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 2,5-difluorobenzoyl 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 0.94 (t, 3 H) 1.33-1.41 (m, 2 H) 1.60-1.69 (m, 2 H) 2.19 (s, 3 H) 2.22 (s, 3 H) 3.93-4.00 (m, 2 H) 6.38 (s, 1 H) 7.24-7.35 (m, 2 H) 7.51-7.59 (m, 1 H); MS (ESI) m/z 324 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08481574B2 |
|---|
| Source dataset | uspto-grants-2013_07 |
|---|
| ORD ID | ord-9eb756d5ae694eaea38537c97cefcdda |
|---|
| Source note | uspto-grants-2013_07 |
|---|