Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTriphenylphosphineHCID 11776—
Reactant4-Carboxyphenylboronic AcidHCID 312183—
Reactant1,4-Dioxaspiro[4.5]dec-7-en-8-yl trifluoromethanesulfonateHCID 11483086—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventDimethylformamideHCID 6228—
Product4-(1,4-Dioxaspiro[4.5]dec-7-en-8-yl)benzoic acidHCID 5955609538.4%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659294B2
Source datasetuspto-grants-2010_02
ORD IDord-0e489130b3e44dfe81078b3cabfffdd1
Source noteuspto-grants-2010_02