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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723960Generated: October 30, 2026

Water → HCID 76585889, compound

https://huagongshe.com/reaction/1723960

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHCID 76565468HCID 76565468—
ReactantHCID 178418361HCID 178418361—
CatalystChlorotris(triphenylphosphine)rhodium(I)HCID 84599—
SolventBenzeneHCID 241—
ProductHCID 76585889HCID 76585889—

Reaction Steps

A solution of {2R-[2α[2′R*, 5′R*(R*)],5β[1(S*), 2R*, 11R*]}-3-{2-[(1,1-dimethylethyl)diphenylsilyloxy]-11-methoxymethyloxy-11-[octahydro-5′-(1-(methoxymethyloxy)undec-3-ynyl) [2.2′-bifuran]-5-yl]-6-undecen-8-ynyl}-5-methyl-2-(5H)-furanone (64 mg, 70 mmole) in benzene (0.5 mL) is stirred at room temperature under a flow of nitrogen while tris(triphenylphosphine)rhodium chloride (14 mg, 15 mmole) is added. The mixture is charged with hydrogen gas and stirred at room temperature for two days. Water is added, and the layers are separated. The aqueous extracted with ethyl acetate (3×2 mL) and the combined organic fractions are washed (1×20 mL water) dried (saturated aqueous NaCl, sodium sulfate), filtered, and concentrated. Chromatography (hexane-2:1 hexane:ethyl acetate gradient over silica gel 230-400 mesh) affords the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07485283B2
Source datasetuspto-grants-2009_02
ORD IDord-91ee0fade6d44c288f507e4381bc79b0
Source noteuspto-grants-2009_02