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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186950Generated: November 1, 2026

Tetramethyltin → 5-(2-hydroxyethyl)-6-methyl-2-benzofuran-1(3H)-one

https://huagongshe.com/reaction/1186950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetramethyltinHCID 11661—
ReactantTriphenylphosphineHCID 11776—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
Reactant5-(2-hydroxyethyl)-6-iodo-2-benzofuran-1(3H)-oneHCID 66643870—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventAmmonium ChlorideHCID 25517—
Product5-(2-hydroxyethyl)-6-methyl-2-benzofuran-1(3H)-oneHCID 66644035—

Reaction Conditions

Temperature50 °C

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 cooled to room temperature, 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 5-(2-hydroxyethyl)-6-methyl-2-benzofuran-1(3H)-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673920B2
Source datasetuspto-grants-2014_03
ORD IDord-d12525b4de434726b887d87badc1732a
Source noteuspto-grants-2014_03