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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404356Generated: October 29, 2026

Water → HCID 57467625, compound

https://huagongshe.com/reaction/404356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
ReactantMethyl 3-bromo-4-(tetrahydro-2H-pyran-2-yloxy)benzoateHCID 57467623—
Catalystpalladium(II) acetateHCID 167845—
ProductHCID 57467625HCID 57467625495.1%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of methyl 3-bromo-4-(tetrahydro-2H-pyran-2-yloxy)benzoate T3.2 (0.500 g, 1.6 mmol), palladium acetate (0.036 g, 0.16 mmol), S-Phos (0.13 g, 0.32 mmol) and tripotassium phosphate (0.32 mL, 4.0 mmol) in DMF (10.00 mL, 129 mmol) and water (0.40 mL, 22 mmol) was stirred. The mixture was purged with nitrogen and placed under vacuum and the process repeated three times. Before heating, 2-methylprop-1-enylboronic acid (0.24 g, 2.4 mmol, commercially available from Synthonix, Cat. No. D3007G1) was added, and the mixture was heated to 70° C. and stirred for 23 hours. The mixture was then cooled to room temperature, diluted with brine, and extracted three times with EtOAc. After drying over anhydrous magnesium sulfate and filtering, the organic solvent was removed under reduced pressure and the product was then purified on silica gel (0-10% EtOAc in hexanes) to yield T23.1 as a colorless oil (0.460 g, 100% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748462B2
Source datasetuspto-grants-2014_06
ORD IDord-37fefcee4f524393adaee816d4e3184a
Source noteuspto-grants-2014_06