HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050490Generated: October 30, 2026
Trifluoroacetic acid → HCID 20058295, compound
https://huagongshe.com/reaction/2050490
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 20058288 | HCID 20058288 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 20058295 | HCID 20058295 | — |
Reaction Steps
To a stirred suspension of this pyridinium chloride (1 mmol) in dichloromethane (5 ml) at 0° C. was added sufficient trifluoroacetic acid to give a clear solution. A solution of m-chloroperoxybenzoic acid (1 mmol) in dichloromethane (2 ml) was added over about 1 minute and the mixture was allowed to warm to room temperature. After 30 minutes, further m-chloroperoxybenzoic acid (1 mmol) in dichloromethane (2 ml) was added. After a further 15 minutes the solvent was removed by evaporation under reduced pressure and the residue was triturated with ethyl acetate to give 1-(5-methoxypyran-4-on-2-yl)4-methylsulphinylpyridinium chloride as a crude gum (which was used in this form for the reaction of Example 32); (DMSO-d6) 3.00(s,3H); 3.65(s,3H); 6.0(s,2H); 6.70(s,1H); 8.15(s,1H); 8.55(d,2H); 9.42(d,2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05013730 |
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| Source dataset | uspto-grants-1991_05 |
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| ORD ID | ord-177a2488b3854cfdb64d755d1a30c1be |
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| Source note | uspto-grants-1991_05 |
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