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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337551Generated: October 25, 2026

Sodium Carbonate → 1,1-Dimethylethyl cyclopropyl[(2,3-dichloro-5-ethenylphenyl)methyl]carbamate

https://huagongshe.com/reaction/337551

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTriphenylphosphineHCID 11776—
Reactant2-Ethenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 5233012—
Reactant1,1-Dimethylethyl[(5-bromo-2,3-dichlorophenyl)methyl]cyclopropylcarbamateHCID 86651660—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
Solvent1-PropanolHCID 1031—
SolventDimethylformamideHCID 6228—
Product1,1-Dimethylethyl cyclopropyl[(2,3-dichloro-5-ethenylphenyl)methyl]carbamateHCID 66895414—

Reaction Conditions

Temperature90 °C

Reaction Steps

1,1-Dimethylethyl[(5-bromo-2,3-dichlorophenyl)methyl]cyclopropylcarbamate (1 eq.) from the previous step and 2-ethenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (1 eq.) were combined in a 2:1 (v/v) mixture of DMF:n-PrOH (0.1 M). To this solution was then added palladium(II) acetate (0.05 eq.) and triphenylphosphine (0.15 eq.) before the vessel was repeatedly evacuated and back-filled with nitrogen. Finally, 2 N aq. Na2CO3 (2 eq.) was added and the resulting biphasic suspension was heated at 90° C. for 18 h. The now black suspension was cooled to RT, diluted with water and extracted with 1:1 (v/v) hexanes:ether. The combined organic extracts were then washed further with 1 N aq. NaOH, water and brine. This was then dried over Na2SO4, filtered and the filtrate concentrated in vacuo to afford a pale yellow oil. Purification of the crude product thus obtained by way of flash chromatography (SiO2, Hex→9:1 (v/v) Hex:EtOAc) afforded the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889714B2
Source datasetuspto-grants-2014_11
ORD IDord-af88e6ed50ec483dbfe8b8c842d3812f
Source noteuspto-grants-2014_11