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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766902Generated: October 30, 2026

Tributylstannane → HCID 178462418, compound

https://huagongshe.com/reaction/1766902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylstannaneHCID 5948—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 178459899HCID 178459899—
CatalystHCID 178418476HCID 178418476—
SolventHexaneHCID 8058—
ProductHCID 178462418HCID 17846241881%

Reaction Steps

A chemical reaction was carried out according to a similar procedure to that described in Example 11-(4) using (1R,2R)-2-[[trans-2-[(1E,3E)-4-(4-cyano-2-fluorophenyl)-1,3-butadienyl]-1,3-dioxan-5-yl]thio]1-(2,4-difluorophenyl)-1-[(1H-1,2,4-triazol-1-yl)methyl]propyl 2-[(allyloxycarbonyl)oxymethyl]benzoate (1.52 g, 2.00 mmol), bis(triphenylphosphine)dichloropalladium (5 mg), and tributyltin hydride (620 mg, 2.13 mmol). The obtained crude product was subjected to chromatography on a silica gel (50 g) column (eluent; ethyl acetate:hexane=1:1˜1:0) to afford the title compound (1.096 g, 81% yield) as a colorless amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230023B2
Source datasetuspto-grants-2007_06
ORD IDord-d2f7f0f0d52949cb9c679acbcfa0a8d7
Source noteuspto-grants-2007_06