HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986699Generated: October 30, 2026
p-Toluenesulfonic acid → HCID 20157034, compound
https://huagongshe.com/reaction/986699
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Reactant | HCID 13338867 | HCID 13338867 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 20157034 | HCID 20157034 | — |
Reaction Steps
In methylene chloride (30 ml) was dissolved 4-[3-(4-acetyl-3-hydroxy-2-propylphenoxy)propoxy]-3-bromobenzoic acid (1.35 g). To the solution were added dihydropyran (0.9 ml) and p-toluene sulfonic acid.monohydrate (5 mg). The mixture was stirred at room temperature for 30 minutes, to which was further added methylene chloride (30 ml). The resulting solution was washed with an aqueous solution of sodium hydrogen carbonate and then with water, followed by drying with sodium sulfate. The solvent was evaporated off, and the residue was purified by means of a silica-gel column chromatography (Developing solvent: chloroform) to give 1.4 g of tetrahydropyranyl 4-[3-(4-acetyl-3-hydroxy-2-propylphenoxy)propoxy]-3-bromobenzoate as colorless oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04714774 |
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| Source dataset | uspto-grants-1987_12 |
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| ORD ID | ord-8c58465b37b6406998028a61b7e271bf |
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| Source note | uspto-grants-1987_12 |
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