HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716294Generated: October 31, 2026
4-(p-Tolyloxy)aniline → HCID 68512931, compound
https://huagongshe.com/reaction/1716294
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(p-Tolyloxy)aniline | HCID 94519 | — |
| Reactant | 5-Bromo-2-methoxypyridine-3-carbaldehyde | HCID 1516403 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 68512931 | HCID 68512931 | — |
Reaction Steps
A solution of 5-bromo-2-methoxy-pyridine-3-carbaldehyde (0.87 g, 4.03 mmol) in dry MeOH (15 mL) was treated with 4-p-tolyloxy-phenylamine (0.88 g, 4.43 mmol) and reflux for 2.5 h. The solution was cooled to 0° C. and treated slowly with NaBH4 (0.38 g, 10.1 mmol). The reaction stirred at room temperature overnight. Additional NaBH4 (0.38 g, 10.1 mmol) was added and the reaction was continued stirring for additional 6 h. The solvent was removed and the residue was partitioned between CH2Cl2 (20 mL) and water (10 mL). The organic portion was brought to the usual work-up to give a crude material. The product was yielded after chromatography purification (silica gel, 25% EtOAc/hexanes). MS (EI) 399, 401 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07803793B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-6a3c5efd0a644e5d901c45ad6e36b609 |
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| Source note | uspto-grants-2010_09 |
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