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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015368Generated: October 31, 2026

Triphenylphosphine → HCID 67302000, compound

https://huagongshe.com/reaction/1015368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantEthyl 4-hydroxycyclohexanecarboxylateHCID 86973—
Reactant2,6-DifluorophenolHCID 94392—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
SolventTolueneHCID 1140—
ProductHCID 67302000HCID 6730200034%

Reaction Conditions

Temperature0 °C

Reaction Steps

4-Hydroxycyclohexanecarboxylic acid ethyl ester (300 mg; 1.7 mmol), triphenylphosphine (1 g; 4.2 mmol) and 2,6-difluorophenol (340 mg; 2.6 mmol) were stirred in anhydrous toluene and chilled to 0° C. under nitrogen flow. Diethyl azodicarboxylate (2 mL; 4.3 mmol) was added to the mixture over 1 minute and warmed to room temperature. Reaction continued for 16 hours. Reaction was quenched with water, and mixture was extracted with 4×5 mL with ethyl acetate. Combined organics were washed with brine and dried over MgSO4. Oily residue was triturated with diethyl ether and solids filtered off. Filtrate was concentrated at reduced pressure and purified via flash chromatography using 5-20% ethyl acetate in hexanes to give 162 mg of title compound. (34% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985755B2
Source datasetuspto-grants-2011_07
ORD IDord-eda9ecee2a4f4c428c61ec6e30987edd
Source noteuspto-grants-2011_07