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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669273Generated: October 31, 2026

Triphenylphosphine → HCID 67341070, compound

https://huagongshe.com/reaction/1669273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
Reactant3-(4-Hydroxy-benzoylamino)-propionic acid methyl esterHCID 10632853—
Reactant2-Cyclohexyl-1-[4'-(trifluoromethyl)[1,1'-biphenyl]-4-yl]ethan-1-olHCID 53415981—
SolventTolueneHCID 1140—
ProductHCID 67341070HCID 6734107031.2%

Reaction Steps

A solution of (±)-2-cyclohexyl-1-(4′-trifluoromethyl-biphenyl-4-yl)-ethanol (0.184 g, 0.527 mmol), 3-(4-hydroxy-benzoylamino)-propionic acid methyl ester (0.136 g, 0.608 mmol), and triphenylphosphine (0.208 g, 0.791 mmol) in toluene (8.0 mL) is treated with 1,1′-(azodicarbonyl)dipiperidine (ADDP, 0.206 g, 0.817 mmol) and stirred overnight. The reaction mixture is filtered through Celite® diluted with EtOAc, washed with water (2×), brine (1×), dried over MgSO4, filtered, and conc. The residue is loaded onto silica gel and eluted with hexanes using a gradient of 25% EtOAc to 100% EtOAc giving (±)-3-{4-[2-cyclohexyl-1-(4′-trifluoromethyl-biphenyl-4-yl)-ethoxy]-benzoylamino}-propionic acid methyl ester (0.091 g, 31%) as a white foam. MS (ES): 554.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989457B2
Source datasetuspto-grants-2011_08
ORD IDord-5a40b1a5ac064cec83fda561578cbbf6
Source noteuspto-grants-2011_08