HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051164Generated: October 27, 2026
Sulfuric Acid → 5-Acetoxypyran-4-one-2-carbonyl chloride
https://huagongshe.com/reaction/2051164
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Comenic acid | HCID 68139 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Acetoxypyran-4-one-2-carbonyl chloride | HCID 10889329 | — |
Reaction Steps
2-Carboxy-5-hydroxypyran-4-one (20 mmole) (Chem.Abs., 1948,42,567; J. Gen. Chem., 1946,16, 2025), acetic anhydride (10 ml) and concentrated sulphuric acid (0.5 ml) were heated to reflux temperature. On cooling to 0° C., the 5-acetoxy compound crystallised (recrystallised from ethanol); δ(DMSO-d6); 2.27(s,3H); 7.05(s,1H); 8.10(s,1H). This compound (5 mmole) was treated with oxalyl chloride (10 mmole) in dichloromethane (5 ml) containing dimethylformamide (15 μl). After 30 minutes the solvent was evaporated, the residue dissolved in toluene (evaporated several times to remove oxalyl chloride) and on final evaporation crystallised to give 5-acetoxypyran-4-one-2-carbonyl chloride which was used directly.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05017569 |
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| Source dataset | uspto-grants-1991_05 |
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| ORD ID | ord-e1fbcf46197543edb0e9767fbe911472 |
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| Source note | uspto-grants-1991_05 |
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