HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443418Generated: October 30, 2026
Sodium Carbonate → 4-(1,4-Dioxaspiro[4.5]dec-7-en-8-yl)benzoic acid
https://huagongshe.com/reaction/1443418
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 4-Carboxyphenylboronic Acid | HCID 312183 | — |
| Reactant | 1,4-Dioxaspiro[4.5]dec-7-en-8-yl trifluoromethanesulfonate | HCID 11483086 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(1,4-Dioxaspiro[4.5]dec-7-en-8-yl)benzoic acid | HCID 59556095 | 38.4% |
Reaction Steps
To a solution of 4-carboxyphenylboronic acid (0.69 g, 3.53 mmol) and 1,4-dioxaspiro[4.5]dec-7-en-8-yl trifluoromethanesulfonate (1.02 g, 3.53 mmol) in 14 mL of DMF were added 7 mL of 2 N aqueous solution of Na2CO3, triphenylphosphine (159 mg, 0.61 mmol), and tris(dibenzylideneacetone)dipalladium(0) (68 mg, 74.2 μmol). After stirring at 80° C. for 3 h and then at rt for 16 h, the mixture was concentrated and partitioned between 100 mL of Et2O and 150 mL of H2O. The aqueous layer was separated and acidified to pH ˜2-3 using concentrated HCl, and extracted with CH2Cl2 (2×100 mL). The organic layers were combined, dried over Na2SO4, and concentrated. The residue was re-crystallized from 10 mL of EtOAc to give 353 mg (38%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07659294B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-0e489130b3e44dfe81078b3cabfffdd1 |
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| Source note | uspto-grants-2010_02 |
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