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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475585Generated: October 30, 2026

Tributylphosphine → HCID 57855825, compound

https://huagongshe.com/reaction/475585

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant2-IndanolHCID 77936—
ReactantHCID 68983174HCID 68983174—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57855825HCID 57855825—

Reaction Conditions

Temperature50 °C

Reaction Steps

A 0.26 g quantity of 3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(3-methylpyridin-2-yl)propan-1-one obtained in Example 136 was dissolved in 10 ml of tetrahydrofuran. To the obtained solution were added 0.2 g of 2-hydroxyindane, 0.75 ml of diisopropyl azodicarboxylate (40% toluene solution) and 0.31 g of tri(n-butyl)phosphine, and the mixture was stirred at 50° C. After 3 hours, 0.2 g of 2-hydroxyindan, 0.75 ml of diisopropyl azodicarboxylate (40% toluene solution) and 0.31 g of tri(n-butyl)phosphine were further added thereto, and the mixture was stirred at 50° C. overnight. The reaction mixture was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane:ethyl acetate:dichloromethane=1:1:1), and recrystallized from acetone/diisopropyl ether to give 0.13 g of colorless powdery 3-{2-[3-(indan-2-yloxy)-4-methoxyphenyl]oxazol-4-yl}-1-(3-methylpyridin-2-yl)propan-1-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637559B2
Source datasetuspto-grants-2014_01
ORD IDord-dff1a755ec1946a6bd831f44857a6dd9
Source noteuspto-grants-2014_01