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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | Methyl 4-bromo-3-(2-methylallyloxy)benzoate | HCID 57662790 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Methyl 3,3-dimethyl-2,3-dihydrobenzofuran-6-carboxylate | HCID 58279528 | 36.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08476430B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-996333d3dab945a2b15b8db6326aa00a |
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| Source note | uspto-grants-2013_07 |
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