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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773972Generated: November 1, 2026

4-Bromo-2-chloro-1-cyclopropoxybenzene → Tert-butyl 2-(3-chloro-4-cyclopropoxyphenyl)acetate

https://huagongshe.com/reaction/1773972

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-2-chloro-1-cyclopropoxybenzeneHCID 57594658—
ReactantHCID 178451183HCID 178451183—
CatalystHCID 178418851HCID 178418851—
Solvent1,4-DioxaneHCID 31275—
ProductTert-butyl 2-(3-chloro-4-cyclopropoxyphenyl)acetateHCID 89649373—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 4-bromo-2-chloro-1-cyclopropoxy-benzene (610 mg, 2.46 mmol, 1.00 eq.) in dioxane (20 mL), bis(tri-t-butylphosphine)palladium (0) (193 mg, 0.37 mmol, 0.15 eq.) and 2-tert-butoxy-2-oxoethylzinc chloride (0.5M in diethyl ether) (8.9 mL, 4.44 mmol, 1.80 eq.) were added in sequence. The resulting mixture was stirred at r.t. for 18 hours and further at 60° C. for 4 hours. The mixture was allowed to cool down to r.t. and filtered through Celite. The filtrate was concentrated in vacuo. The residue was purified by flashmaster (column: 100 g, flow: 45 mL/min, 40 fractions of 45 mL, Heptane to Heptane+5% AcOEt) to yield the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09255090B2
Source datasetuspto-grants-2016_02
ORD IDord-f19b22be283240fe8b52cd77b05a1b92
Source noteuspto-grants-2016_02