HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257170Generated: October 25, 2026
4-Hydroxybenzaldehyde → 4-[2-(N-Methyl-N-(2-benzoxazolyl)amino)ethoxy]benzaldehyde
https://huagongshe.com/reaction/257170
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 2-(Benzooxazol-2-yl-methyl-amino)-ethanol | HCID 10241663 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-[2-(N-Methyl-N-(2-benzoxazolyl)amino)ethoxy]benzaldehyde | HCID 10040213 | — |
Reaction Steps
To a solution of 2-[N-methyl-N-(2-benzoxazolyl) amino]ethanol (9.6 g), triphenylphosphine (13.1 g) and 4-hydroxybenzaldehyde (6.1 g) in dry tetrahydrofuran (150 ml) was added dropwise a solution of diethyl azodicarboxylate (9.0 g) in dry tetrahydrofuran (30 ml), under a blanket of nitrogen with stirring at room temperature. The solution was stirred overnight at room temperature following which the solvent was removed under reduced pressure. The residue was dissolved in diethyl ether (300 ml), filtered and the ether solution was washed with dilute sodium hydroxide solution (200 ml), saturated brine (200 ml), dried (MgSO4), filtered and the solvent evaporated. The title compound (mp 97°-98° C.) was obtained after chromatography on silica-gel, eluting with dichloromethane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05260445 |
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| Source dataset | uspto-grants-1993_11 |
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| ORD ID | ord-c7b0f98e6b27484d8b7cb8160d65ddb3 |
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| Source note | uspto-grants-1993_11 |
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