HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111053Generated: October 25, 2026
Phloroglucinol → 1,3,5-Tris(vinyloxy)benzene
https://huagongshe.com/reaction/2111053
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phloroglucinol | HCID 359 | — |
| Reactant | Vinyl Acetate | HCID 7904 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1-Hydroxy-3,5-bis(vinyloxy)benzene | HCID 22935762 | — |
| Reactant | 1,3-Dihydroxy-5-vinyloxybenzene | HCID 22935814 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1,3,5-Tris(vinyloxy)benzene | HCID 11820226 | — |
Reaction Steps
To a mixture of di-μ-chlorobis(1,5-cyclooctadiene)diiridium(I) [Ir(cod)Cl]2 (67 mg, 0.1 mmol) and sodium carbonate (640 mg, 6 mmol) in toluene (5 ml) were added 1,3,5-trihydroxybenzene (5 mmol) and vinyl acetate (2.15 g, 25 mmol), followed by stirring at 100° C. in an atmosphere of argon gas for 6 hours. The reaction mixture was analyzed by gas chromatography to find that 1,3-dihydroxy-5-vinyloxybenzene, 1-hydroxy-3,5-bis(vinyloxy)benzene, and 1,3,5-tris(vinyloxy)benzene were formed in yields of 5%, 4%, and 18%, respectively, with a conversion from 1,3,5-trihydroxybenzene of 29%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07518021B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-2a8a427d2684410f82b3555cd7176b78 |
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| Source note | uspto-grants-2009_04 |
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