HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 380138Generated: October 30, 2026
p-Toluenesulfonic acid → HCID 18367277, compound
https://huagongshe.com/reaction/380138
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 5-Methoxytetralone | HCID 36620 | — |
| Reactant | HCID 541979 | HCID 541979 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 18367277 | HCID 18367277 | 46.4% |
Reaction Steps
A solution of 5-methoxy-1-oxo-1,2,3,4-tetrahydronaphthalene (0.67 g), 1-(4,5-diphenyloxazol-2-yl)ethylamine (0.98 g) and p-toluenesulfonic acid (catalytic amount) in toluene (30 ml) was refluxed for 7 hours with Dean-stark equipment. The solution was evaporated in vacuo and methanol (MeOH) (10 ml) was added to the residue. To the MeOH solution, NaBH4 (0.21 g) was added at 0° C. After being stirred for 2 hours at room temperature, the solution was evaporated in vacuo. The residue was partitioned between ethyl acetate and water. The organic layer was washed with brine. The dried solvent was evaporated in vacuo, and the residue was purified by chromatography on silica gel to give 1-[1-(4,5-diphenyloxazol-2-yl)ethylamino]-1,2,3,4-tetrahydro-5-methoxynaphthalene (0.73 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06300344B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-5e0cd79afafd4413a189599b46a2867a |
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| Source note | uspto-grants-2001_10 |
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