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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092263Generated: October 31, 2026

Water → HCID 66591140, compound

https://huagongshe.com/reaction/1092263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
ReactantHCID 66591461HCID 66591461—
ReactantHCID 86618118HCID 86618118—
CatalystHCID 178418397HCID 178418397—
SolventPotassium Phosphate, TribasicHCID 62657—
ProductHCID 66591140HCID 6659114078%

Reaction Conditions

Temperature80 °C

Reaction Steps

278 mg (1.20 mmol, 1.5 eq) of methyl 3-(5-bromofuran-2-yl)acrylate and 300 mg (0.80 mmol, 1.0 eq) of octanoylmethyl-[3-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)benzyl]amide (prepared as in 1 e) are dissolved in 5 ml of a 5/1 mixture of dimethylformamide and of 2M potassium phosphate solution. 46 mg (0.04 mmol, 5 mol %) of tetrakis(triphenylphosphine)palladium are added and the reaction mixture is then stirred for 2 hours at 80° C. The reaction is stopped by adding 30 ml of water and is then extracted with ethyl acetate. The organic phases are combined and dried over sodium sulfate. The solvents are evaporated off and the residue is then chromatographed on silica gel (80/20 to 60/40 heptane/ethyl acetate). 250 mg of methyl 3-(5-{3-[(methyloctanoylamino)methyl]phenyl}furan-2-yl)acrylate are obtained. Yield=78%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129416B2
Source datasetuspto-grants-2012_03
ORD IDord-08a9b6992e0e46f69a2b2d3862c0be42
Source noteuspto-grants-2012_03