HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1446648Generated: November 1, 2026
Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) → HCID 21024034, compound
https://huagongshe.com/reaction/1446648
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Reactant | (8E,12E,14E)-7-Carbamoyloxy-3,6,21-tri(1-ethoxyethoxy)-6,10,12,16,20-pentamethyl-18,19-epoxytricosa-8,12,14-trien-11-olide | HCID 21024033 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21024034 | HCID 21024034 | 74.1% |
Reaction Steps
Pyridinium p-toluenesulfonate (1.2 mg, 4.8 μmol) was added to a solution of (8E,12E,14E)-7-carbamoyloxy-3,6,21-tri(1-ethoxyethoxy)-6,10,12,16,20-pentamethyl-18,19-epoxytricosa-8,12,14-trien-11-olide (3.6 mg, 4.77 μmol) in methanol (1 mL), followed by stirring at room temperature for 3 hours. The reaction mixture was evaporated, ethyl acetate, water and a saturated sodium bicarbonate aqueous solution were added to the resulting residue, and the mixture was extracted with ethyl acetate. The resulting organic layer was dried over anhydrous magnesium sulfate, filtered and then evaporated. The resulting residue was purified by thin layer chromatography (MERCK Silica gel 60 F254, 0.2 mm, developing solution; methanol-dichloromethane, 1:29) to give the title compound (1.9 mg, 74%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07667052B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-36e688c83b25421a8b159a93aec715c1 |
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| Source note | uspto-grants-2010_02 |
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