HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465764Generated: October 30, 2026
Tetramethyltin → 5-(2-hydroxyethyl)-6-methyl-2-benzofuran-1(3H)-one
https://huagongshe.com/reaction/1465764
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetramethyltin | HCID 11661 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | 5-(2-hydroxyethyl)-6-iodo-2-benzofuran-1(3H)-one | HCID 66643870 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | 5-(2-hydroxyethyl)-6-methyl-2-benzofuran-1(3H)-one | HCID 66644035 | — |
Reaction Steps
To a flask charged with 5-(2-hydroxyethyl)-6-iodo-2-benzofuran-1(3H)-one (6.00 g, 19.7 mmol) and a stir bar was added Pd2(dba)3 (452 mg, 0.493 mmol), PPh3 (1 g, 4 mmol) and NMP (50 mL). The mixture was purged with N2 and heated to 50° C. for 10 min, followed by addition of CuI (375 mg, 1.97 mmol). After the mixture was heated for another 10 min, Sn(CH3)4 (5.30 g, 29.6 mmol) was added into the reaction, and it was heated to 120° C. for 2 h. After cooling to RT, the mixture was diluted with saturated NH4Cl (200 mL) and extracted with EtOAc (3×200 mL). The combined organic layers were washed with water and brine, dried over anhydrous sodium sulfate, filtered and concentrated. The residue was purified by prep-HPLC to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08999991B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-401f3fd6438842ec94e5f2e327a53171 |
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| Source note | uspto-grants-2015_04 |
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