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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2256997Generated: October 26, 2026

Stannane, trimethylphenyl- → HCID 178518632, compound

https://huagongshe.com/reaction/2256997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannane, trimethylphenyl-HCID 123095—
ReactantHCID 178518630HCID 178518630—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178518632HCID 17851863258%

Reaction Steps

To a solution of 4-Bromo-8-chloro-3-hydroxy-2,5-dioxo-2,5-dihydro-1H-benz[b]azepine (400 mg) in THF (10 mL) was added phenyltrimethylstannane (600 mg) and trans-Benzyl(chloro)bis (triphenyl-phosphinepalladium(II) (50 mg). The solution was heated to reflux for 5 hours at which time a dark gray precipitate formed. The reaction mixture was cooled to room temperature and diluted with an ether-tetrahydrofuran mixture (1:1). This mixture was washed with a 10% solution of potassium fluoride, dried (Na2SO4), and evaporated to dryness. Chromatography, with ethyl acetate as the eluent, yielded the title compound as a white solid (230 mg); mp 193-196 degrees C.; NMR: 7.18(m,2H), 7.31(m, 4H), 7.52(s, 1H), 7.87(d, 1H, J=8.7), 10.28(brs, 1H), 11.81(s, 1H). Analysis for C16H10ClNO3 -0.3H2O: Calculated: C, 62.98, H, 3.50, N, 4.59: Found: C, 62.82, H, 3.33, N, 4.67.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05656626
Source datasetuspto-grants-1997_08
ORD IDord-fb18654225c24395a3507f4ca55c53d9
Source noteuspto-grants-1997_08