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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 445921Generated: October 29, 2026

Tributylstannane → Methyl 3,3-dimethyl-2,3-dihydrobenzofuran-6-carboxylate

https://huagongshe.com/reaction/445921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylstannaneHCID 5948—
ReactantAzobisisobutyronitrileHCID 6547—
ReactantEthyl acetate hexaneHCID 21226206—
ReactantMethyl 4-bromo-3-(2-methylallyloxy)benzoateHCID 57662790—
SolventBenzeneHCID 241—
ProductMethyl 3,3-dimethyl-2,3-dihydrobenzofuran-6-carboxylateHCID 5827952836.2%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of methyl 4-bromo-3-(2-methylallyloxy)benzoate (0.500 g, 1.754 mmol), tributyltin hydride (0.708 mL, 2.63 mmol), and AIBN (0.035 g, 0.210 mmol) in benzene (20 mL) was heated in a pressure tube at 120° C. for 22 h. The volatiles were removed under vacuum. The residue was diluted with ethyl acetate (100 mL) and shaken with 10% KF solution. The resulting precipitate was removed by suction filtration through CELITE®. The organic layer of the filtrate was separated, washed with saturated NaHCO3 solution and brine, and dried over anhydrous MgSO4. The desired product, methyl 3,3-dimethyl-2,3-dihydrobenzofuran-6-carboxylate (0.131 g, 0.635 mmol, 36.2% yield) was isolated as a colorless oil with ISCO (40 g silica gel, 1-10% ethyl acetate/hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476430B2
Source datasetuspto-grants-2013_07
ORD IDord-996333d3dab945a2b15b8db6326aa00a
Source noteuspto-grants-2013_07