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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Fluoro-2-methylbenzoyl chloride | HCID 2737383 | — |
| Reactant | 3-Butyl-2,4,5-trimethylthiazol-3-ium iodide | HCID 69165591 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Product | HCID 69188065 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481574B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-6d99893b04794dc892e89e05f8b5b019 |
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| Source note | uspto-grants-2013_07 |
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