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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010877Generated: October 30, 2026

Stannane, tributyl(1-ethoxyethenyl)- → HCID 125496709, compound

https://huagongshe.com/reaction/1010877

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannane, tributyl(1-ethoxyethenyl)-HCID 619414—
Reactant(S)-tert-Butyl (1-(4-bromophenyl)ethyl)carbamateHCID 56973617—
CatalystHCID 178418476HCID 178418476—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 125496709HCID 125496709—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 600 mg of the compound [1-1], 75 mg of dichlorobis(triphenylphosphine)palladium (II), 743 μL of tributyl (1-ethoxyvinyl)tin, and 3 mL of 1,4-dioxane, was stirred overnight at 100° C. After standing to cool, the insolubles were filtered and the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=8/2) to obtain 367 mg of tert-butyl[(1S)-1-(4-acetylphenyl)ethyl]carbamate [1-2] (hereinafter, referred to as the compound [1-2]) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977336B2
Source datasetuspto-grants-2011_07
ORD IDord-397c69447bc64d76ad78dbeb45786b65
Source noteuspto-grants-2011_07