HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380390Generated: November 2, 2026
Methanesulfonic Acid → HCID 18955530, compound
https://huagongshe.com/reaction/2380390
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Reactant | HCID 9951074 | HCID 9951074 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 18955530 | HCID 18955530 | 55% |
Reaction Steps
2.41 g (20.0 mmol) of pivaloyl chloride are added dropwise over a period of 10 minutes to a suspension of 2.70 g (10.0 mmol) of 3-(4-ethoxyphenyl)-5-hydroxybenzofuran-2-one (compound (136), Table 1, Example 1) in 10 ml of xylene and 0.1 ml of methanesulfonic acid which is stirred at 95° C. under a nitrogen atmosphere. The clear, homogeneous reaction mixture is then refluxed for 2.5 hours and then concentrated under a slight vacuum. The residue is taken up in dichloromethane and washed with saturated sodium bicarbonate solution and water. The organic phases are combined, dried over sodium sulfate and concentrated on a vacuum rotary evaporator. The residue gives 1.95 g (55%) of 3-(4-ethoxyphenyl)-5-pivaloyloxybenzofuran-2-one, oil (compound (135), Table 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05367008 |
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| Source dataset | uspto-grants-1994_11 |
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| ORD ID | ord-f11057f217d245a48009c30b41a1dd82 |
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| Source note | uspto-grants-1994_11 |
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