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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1053511Generated: November 2, 2026

4-Hydroxybiphenyl → HCID 10560973, compound

https://huagongshe.com/reaction/1053511

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybiphenylHCID 7103—
ReactantPropiolic AcidHCID 10110—
ReactantDicyclohexylcarbodiimideHCID 10868—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDiethyl EtherHCID 3283—
ProductHCID 10560973HCID 1056097390%

Reaction Steps

To an ice cooled and stirred solution of propargylic acid (285 mg, 4.01 mmol) and 4-phenylphenol (693 mg, 4.07 mmol) in dry diethyl ether was added dropwise a solution of N,N′-dicyclohexylcarbodiimide (DCC, 840 mg, 4.07 mmol) and 4-dimethylaminopyridine (DMAP, 3.2 mg, 0.03 mmol) in dry diethyl ether (10 mL) during 2 h under nitrogen atmosphere. Reaction mixture was then stirred at room temperature for 10 h, filtered and the solid was washed with diethyl ether. Then, the combined filtrate was washed with 1 N HCl solution followed by washing with brine and dried with anhydrous Na2SO4. The solvent was removed under reduced pressure to give the crude product that was then purified by column chromatography using ethyl acetate:hexane (1:9) as an eluant to give compound 1 (0.81 mg, 90%). 1H NMR (400 MHz, CDCl3): δ 3.12 (s, 1H), 7.24 (s, 1H), 7.26 (s, 1H), 7.38 (s, 1H), 7.47 (t, J=7.8 Hz, 2H), 7.57 (s, 1H), 7.59 (s, 1H), 7.62 (s, 1H), 7.64 (s, 1H). HRMS ESI (m/z): Calculated for C15H10O2 ([M+H]+): 223.0681. found: 223.0734.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09393306B2
Source datasetuspto-grants-2016_07
ORD IDord-6a3371ba524b42e789b2ab5ac5a49de0
Source noteuspto-grants-2016_07