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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633851Generated: November 1, 2026

Hexane → HCID 86730725, compound

https://huagongshe.com/reaction/633851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant(1,1'-Binaphthalen)-2-yldi-tert-butylphosphineHCID 2734941—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 71118315HCID 71118315—
Catalystpalladium(II) acetateHCID 167845—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86730725HCID 8673072556.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

Potassium tert-butoxide (231 mg, 2.06 mmol, 2.0 eq) is added at room temperature to a stirred solution of (3R,6S)-{[6-[3-(3-chloro-5-fluoro-6-methoxy-quinolin-4-yl)-2,3-dihydroxy-propyl]-tetrahydro-pyran-3-yl}-carbamic acid tert-butyl ester (500 mg, 1.03 mmol, 1.0 eq) in dioxane (50 mL), followed by palladium(II) acetate (93 mg, 0.41 mmol, 0.4 eq) and racemic-2-di-tert-butylphosphino-1,1′-binaphthyl (164 mg, 0.41 mmol, 0.4 eq). After 16 hours stirring at 100° C., the reaction mixture is cooled down to room temperature and filtered through decalite. The filtrate is concentrated and the crude product is purified by column chromatography (silica gel, eluent: n-hexane:ethyl acetate, 5:1, v/v) to afford (3R,6S)-[6-(9-fluoro-1-hydroxy-8-methoxy-1,2-dihydro-furo[2,3-c]quinolin-2-ylmethyl)-tetrahydro-pyran-3-yl]-carbamic acid tert-butyl ester as a yellow solid (260 mg, 56% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321788B2
Source datasetuspto-grants-2016_04
ORD IDord-046d26043d024532929e0d6206320056
Source noteuspto-grants-2016_04