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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691536Generated: November 2, 2026

Tributylphosphine → HCID 59364066, compound

https://huagongshe.com/reaction/1691536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
ReactantHCID 59364062HCID 59364062—
ReactantMethyl 2-(4-hydroxyphenyl)cyclopropane-1-carboxylateHCID 59364069—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
ProductHCID 59364066HCID 5936406690.4%

Reaction Steps

A solution of methyl 2-(4-hydroxyphenyl)cyclopropanecarboxylate (0.157 g, 0.816 mmol), (2′,6′-dimethyl-4′-[(3-methyloxetan-3-yl)methoxy]biphenyl-3-yl}methanol (0.231 g, 0.741 mmol) and tributylphosphine (0.298 g, 1.47 mmol) in toluene (15 mL) was stirred, 1,1′-(azodicarbonyl)dipiperidine (0.372 g, 1.47 mmol) was added, and the mixture was stirred at room temperature for 4 hr. Hexane (15 mL) was added to the reaction mixture, and the precipitated insoluble material was filtrated. The filtrate was concentrated under reduced pressure and the residue was purified by silica gel column chromatography (ethyl acetate:hexane=10:90-40:60) to give the title compound (0.326 g, yield 82%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153694B2
Source datasetuspto-grants-2012_04
ORD IDord-55d80eb1bc22476eada58349975ffa88
Source noteuspto-grants-2012_04