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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276083Generated: October 30, 2026

3-Hydroxybenzaldehyde → HCID 18617256, compound

https://huagongshe.com/reaction/276083

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
ReactantHCID 10487882HCID 10487882—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18617256HCID 18617256—

Reaction Steps

10.00 g (81.89 mmoles) of 3-hydroxybenzaldehyde, 15.49 g (81.89 mmoles) of 2-(2-phenyl-4-oxazolyl)ethanol, and 21.48 g (81.89 mmoles) of triphenylphosphine were dried under vacuum and combined with 200 mL THF under N2. The mixture was treated with 16.12 mL (81.89 mmoles) of diisopropylazodicarboxylate added dropwise over 0.25 hr resulting in a mild exotherm. After stirring for 24 hr at ambient temperature, the crude reaction mixture was concentrated under reduced pressure to a viscous amber oil. The oil was diluted in 300 mL EtOAc, washed with 2.5 N NaOH (3×200 mL), H2O (2×300), and brine 300 mL. The combined organics were dried over MgSO4 and concentrated under reduced pressure again to a viscous amber oil. The reaction mixture was separated using silica gel column chromatography (6:1 Hex:EtOAc) from which the product was recovered and then recrystallized from iprOH to afford 15.10 g (63.10%.) of white crystalline solid, m.p. 51-53° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06353027B1
Source datasetuspto-grants-2002_03
ORD IDord-d60c110869c941578e50eafdc3b87b34
Source noteuspto-grants-2002_03