HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858142Generated: October 30, 2026
Water → Benzofuran-2,3-dione2-{o-[2-(tetrahydropyran-2-yloxy)-ethyl]-oxime}
https://huagongshe.com/reaction/1858142
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 2-(2-Bromoethoxy)tetrahydro-2H-pyran | HCID 86621 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 178516824 | HCID 178516824 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Benzofuran-2,3-dione2-{o-[2-(tetrahydropyran-2-yloxy)-ethyl]-oxime} | HCID 54456798 | 63.5% |
Reaction Steps
5 g (0.03 mol) of benzofuran-2,3-dione 2-oxime (XI-1) are dissolved in 30 ml of methanol, and at 20° C. 15 ml of a 2 molar solution of sodium methoxide in methanol are added dropwise. The solvent is distilled off under reduced pressure. The crystalline residue is dissolved in 30 ml of N-methyl-2-pyrrolidinone and treated with 6.27 g (0.03 mol) of 2-(2-bromoethoxy)-tetrahydropyran at 20° C. The reaction mixture is stirred for 16 hours at 20° C., poured into 100 ml of water and the resulting mixture is extracted twice with 100 ml of dichloromethane each time. The solvent is distilled off under reduced pressure and the residue is chromatographed over silica gel using a mixture of diethyl ether/dichloromethane/petroleum ether (1:1:2). 5.55 g (62.1% of theory) of benzofuran-2,3-dione 2-{O-[2-(tetrahydropyran-2-yloxy)-ethyl]-oxime} (XIV-2) are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06150521 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-b079f36f6f384594828f9f54c71fe37b |
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| Source note | uspto-grants-2000_11 |
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