HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276083Generated: October 30, 2026
3-Hydroxybenzaldehyde → HCID 18617256, compound
https://huagongshe.com/reaction/276083
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Hydroxybenzaldehyde | HCID 101 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | HCID 10487882 | HCID 10487882 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18617256 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06353027B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-d60c110869c941578e50eafdc3b87b34 |
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| Source note | uspto-grants-2002_03 |
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