Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454191Generated: October 26, 2026

Hydrochloric Acid → HCID 57529321, compound

https://huagongshe.com/reaction/1454191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantButyl vinyl etherHCID 8108—
ReactantPotassium CarbonateHCID 11430—
Reactant1,3-Bis(diphenylphosphino)propaneHCID 81219—
ReactantMethyl 3-bromo-5-(methyl(propyl)carbamoyl)benzoateHCID 57529325—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 57529321HCID 5752932163.1%

Reaction Conditions

Temperature122 °C

Reaction Steps

A mixture of methyl 3-bromo-5-(methyl(propyl)carbamoyl)benzoate (314 mg, 1.0 mmol), 1-(vinyloxy)butane (200.4 mg, 0.26 mL, 2.0 mmol), palladium acetate (6.68 mg, 0.030 mmol), DPPP (27.2 mg, 0.066 mmol) and potassium carbonate (166 mg, 1.2 mmol) in DMF (2.5 mL) and H2O (0.3 mL) in a Smith process vial was heated at 122° C. in microwave for 3 h. The reaction mixture was cooled down to RT and hydrolyzed by addition of 5% HCl slowly. The reaction mixture was worked up by extraction with ethyl acetate and concentration under vacuum. The crude mixture was purified by reverse phase prep HPLC to give the title compound (175 mg, 63% yield): HPLC retention time: 1.58 min (method A). MS (ESI) (M+H)+ 278.19.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07476764B2
Source datasetuspto-grants-2009_01
ORD IDord-999ee1499afc4e6fa61cc8c9b66d6719
Source noteuspto-grants-2009_01