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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 914517Generated: October 31, 2026

4-Hydroxybiphenyl → HCID 59759083, compound

https://huagongshe.com/reaction/914517

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybiphenylHCID 7103—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
ReactantHCID 67396216HCID 67396216—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59759083HCID 597590833%

Reaction Steps

To a suspension of 2-{[4-(2-hydroxyethyl)-1,3-thiazol-2-yl]thio}-2-methylpropionic acid resin (0.3 g) synthesized in Example 713-1 in tetrahydrofuran (3.0 mL) were added triphenylphosphine (0.12 g) and 4-phenylphenol (0.17 g), and the mixture was left standing for 15 min. Thereto was added diisopropyl azodicarboxylate (40% toluene solution, 0.26 ml), and the mixture was stirred at room temperature for 30 min. The resin was collected by filtration from the reaction mixture, and washed three times with tetrahydrofuran. This operation was repeated three times, and the obtained resin was washed three times each with dimethylformamide, tetrahydrofuran and methanol, and vacuum dried. To the resin was added trifluoroacetic acid, and the mixture was left standing at room temperature for 4 hr. The resin was filtered off and the filtrate was concentrated by blowing nitrogen gas thereto, and purified by HPLC to give the title compound (0.012 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026370B2
Source datasetuspto-grants-2011_09
ORD IDord-1ff89335f1084edd922951641d18654e
Source noteuspto-grants-2011_09