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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2257002Generated: October 30, 2026

2-(Tributylstannyl)furan → HCID 178518634, compound

https://huagongshe.com/reaction/2257002

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tributylstannyl)furanHCID 4393688—
ReactantHCID 18980002HCID 18980002—
CatalystTris(furan-2-yl)phosphaneHCID 521585—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductHCID 178518634HCID 17851863455.2%

Reaction Steps

A solution of tri(2-furyl)phosphine (0.026 g) and tris(dibenzylideneacetone)dipalladium (O) (0.026 g) in toluene (50 mL) was allowed to stir for 10 minutes. To this solution was added 8-chloro-4-iodo-3-methoxy-2,5-dioxo-2,5-dihydro-1H-benz-[b]azepine (1.0 g), followed by 2-tributylstannylfuran (1.2 g). The reaction was heated to reflux for 0.5 hour, was allowed to cool, and the toluene was evaporated. The residue was triturated with hot hexanes (75 mL). The isolated solid was recrystallized from ethyl acetate/hexanes (1:1) to afford the title compound (0.44 g); mp 233°-234° C.; NMR: 11.47 (bs, 1), 7.79 (s, 1), 7.58 (d, 1, J=8.9), 7.34-7.31 (m, 2), 6.91 (d, 1, J=3.4), 6.61 (m, 1), 3.82 (s, 3). Analysis for C15H10ClNO4 0.5 H2O.: Calculated: C, 57.61; H, 3.54; N, 4.47; Found C, 57.77; H, 3.13; N, 4.46.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05656626
Source datasetuspto-grants-1997_08
ORD IDord-60e33a0fd65649e8862932496323fc49
Source noteuspto-grants-1997_08