HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568068Generated: October 30, 2026
p-Toluenesulfonic acid → HCID 9884605, compound
https://huagongshe.com/reaction/568068
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | HCID 15383994 | HCID 15383994 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 9884605 | HCID 9884605 | 43.6% |
Reaction Steps
A few mg of toluene-4-sulphonic acid are added to a solution of 7 g of 3-[1-(4-fluorophenyl)-1-hydroxy-1-(4-methanesulphonylphenyl)methyl]dihydrofuran-2-one, prepared in Example 3, in 100 ml of toluene and the mixture is refluxed for 10 hours in a Dean-Stark apparatus. The solvent is then evaporated off to dryness under vacuum and the residue is chromatographed using a 9/1 dichloromethanel/acetone mixture as the eluent to give an oil, which is chromatographed using t-butyl methyl ether as the eluent to give 2.9 g of (E)-3-[1-(4-fluorophenyl)-1-(4-methanesulphonylphenyl)methylidene]dihydrofuran-2-one (second product eluted) in the form of crystals melting at 187-9° C. 1.5 g of (Z)-3-[1-(4-fluorophenyl)-1-(4-methanesulphonylphenyl)methylidene]dihydrofuran-2-one (first product eluted) are recovered in the form of crystals melting at 157-158° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06180651B2 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-98a33111491e4604bb0793dbe2d30b0b |
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| Source note | uspto-grants-2001_01 |
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