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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373036Generated: October 26, 2026

Tributylphenyltin → HCID 178523764, compound

https://huagongshe.com/reaction/1373036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphenyltinHCID 607632—
ReactantHCID 178523770HCID 178523770—
CatalystHCID 178418476HCID 178418476—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178523764HCID 17852376477.4%

Reaction Steps

Under argon atmosphere, a mixture comprising 1.0 g trans-4-(benzyloxycarbonylamino)cyclohexanecarbonyl chloride, 1.92 g of tributylphenyltin, 61 mg of dichlorobis-(triphenylphosphine)palladium and 10 mL of dioxane was stirred at 110° C. for 12 hours. After cooling, the reaction mixture was concentrated by a centrifugal concentrator, and then, the residue was dissolved in tetrahydrofuran and evaporated to dryness with 5 g of silica gel. The resulting residue was purified by silica gel flash chromatography (solvent: ethyl acetate-hexane (1:2) to (1:1) to obtain 883 mg of N-benzyloxycarbonyl-trans-4-benzoylcylohexylamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07160877B2
Source datasetuspto-grants-2007_01
ORD IDord-29df8a3127cc4c83ad754553a9d354fa
Source noteuspto-grants-2007_01