Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1866538Generated: November 1, 2026

(2,3-Dihydro-1-benzofuran-2-yl)methyl 4-methylbenzene-1-sulfonate → ethyl-dihydrobenzofuran

https://huagongshe.com/reaction/1866538

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2,3-Dihydro-1-benzofuran-2-yl)methyl 4-methylbenzene-1-sulfonateHCID 14099474—
ReactantHCID 178418348HCID 178418348—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDiethyl EtherHCID 3283—
Productethyl-dihydrobenzofuranHCID 1223116998%

Reaction Conditions

Temperature-10 °C

Reaction Steps

Methyl lithium (1.6M in diethyl ether, 313 mL, 500 mmol) was added to a solution of copper (I) iodide (47.6 g, 250 mmol) in diethyl ether (750 mL) at −70° C. The solution was then allowed to warm to −10° C. and was stirred for 30 minutes. The mixture was then added to a solution of 2,3-dihydro-1-benzofuran-2-ylmethyl4-methylbenzenesulfonate (preparation 97) (15.2 g, 50 mmol) in diethyl ether (500 mL) and the reaction mixture was stirred at −40° C. for 1 hour and at room temperature for 2 hours. The mixture was then cooled to −70° C. and quenched with 10% ammonium chloride solution (750 mL) and 2M hydrochloric acid (50 mL), diluted with 0.88 ammonia (100 mL) and then stirred for 18 hours. The reaction mixture was extracted with diethyl ether (3×500 mL) and the organic solution was dried over magnesium sulfate and concentrated in vacuo to afford the title compound as a brown oil in 98% yield, 7.25 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07629358B2
Source datasetuspto-grants-2009_12
ORD IDord-36d112e66d17421bb123d0d57b3685b6
Source noteuspto-grants-2009_12