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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815489Generated: October 29, 2026

Stannous Chloride → HCID 11691222, compound

https://huagongshe.com/reaction/1815489

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannous ChlorideHCID 24479—
ReactantHCID 10696558HCID 10696558—
SolventEthanolHCID 702—
ProductHCID 11691222HCID 1169122244.2%

Reaction Steps

To a stirred solution of nitrobenzene from Example 144A (170 mg, 0.34 mmol) in 2 mL of EtOH was added SnCl2 (325 mg, 1.72 mmol). The mixture was then refluxed under nitrogen atmosphere for 2 hours. The reaction was allowed to cool to ambient temperature, quenched with sat. NaHCO3, extracted with EtOAc(2×20 mL). The combined organic layer was washed with brine, dried over Na2SO4, concentrated in vacuo. The residue was then purified on Gilson preparative HPLC as described in Example 38B to give the title compound (70 mg, 44% yield) as a light yellow solid. 1H NMR (d6-DMSO, 300 MHz) δ 2.04 (s, 3H), 3.42-3.80 (m, 8H), 4.84 (s, 2H), 5.32 (s, 2H), 6.51 (d, J=8.4 Hz, 1H), 6.78 (d, J=8.4 Hz, 2H), 7.26 (d, J=15.6 Hz, 1H), 7.41 (d, J=15.6 Hz, 1H), 7.48 (d, J=8.4 Hz, 1H), 7.95 (d, J=1.8 Hz, 1H). MS (APCI+) (M+H)+ at m/z 465, 467, 469, 471.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878700B1
Source datasetuspto-grants-2005_04
ORD IDord-8f0b409a7e8b4c0f9726cf0b305b0f98
Source noteuspto-grants-2005_04