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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275053Generated: November 4, 2026

3,3-Diethoxy-1-propene → HCID 22118874, compound

https://huagongshe.com/reaction/1275053

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,3-Diethoxy-1-propeneHCID 62477—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant9-Borabicyclo(3.3.1)nonaneHCID 78966—
Reactant7-bromopyrido[2,3-b]pyrazineHCID 4246943—
SolventBenzeneHCID 241—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22118874HCID 22118874—

Reaction Steps

To a solution of 9-BBN (10.2 mL of a 0.5M solution in tetrahydrofuran) at 0° C. was added dropwise 0.77 mL of acrolein diethyl acetal and the mixture allowed to warm slowly to room temperature. After 15 hours, the mixture was diluted with 12 mL dry tetrahydrofuran followed by the sequential addition of potassium phosphate (1.6 g), palladium(1,1'-bis(diphenylphosphino)ferrocenyl) dichloride (160 mg) and 7-bromo-pyrido[2,3-b]pyrazine (924 mg) and then heated to reflux on an oil bath. After 5 hours, the mixture was cooled to 0° C., diluted with 15 mL benzene and the excess reagents quenched by the addition of 2N sodium hydroxide (3.5 mL) and 30% hydrogen peroxide (2.5 mL). The mixture then extracted with ethyl acetate, washed with brine and the concentrate purified by flash chromatography on silica gel (ethyl acetate:hexane, 1:4; then 1:1; then 4:1) to give the title compound (1.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06159975
Source datasetuspto-grants-2000_12
ORD IDord-e7f9829c32e74a57b198afc45ced2a01
Source noteuspto-grants-2000_12