HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 380145Generated: October 30, 2026
Potassium Carbonate → HCID 18367328, compound
https://huagongshe.com/reaction/380145
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromomethyl-4,5-diphenyl-oxazole | HCID 568599 | — |
| Reactant | HCID 18367245 | HCID 18367245 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18367328 | HCID 18367328 | — |
Reaction Steps
A solution of 2-amino-5-t-butyldiphenylsilyloxy-1,2,3,4-tetrahydronaphthalene (0.96 g), (4,5-diphenyloxazol-2-yl)methyl bromide (0.80 g) and potassium carbonate (0.41 g) in DMF (14 ml) was stirred for 3.5 hours at room temperature. The mixture was partitioned between ethyl acetate and water. The organic layer was washed with brine. The dried solvent was evaporated in vacuo to give crude 2-[(4,5-diphenyloxazol-2-yl)methylamino]-1,2,3,4-tetrahydro-5-t-butyldiphenylsilyloxynaphthalene. To a solution of crude 2-[(4,5-diphenyloxazol-2-yl)methylamino]-1,2,3,4-tetrahydro-5-t-butyldiphenylsilyloxynaphthalene in THF (5 ml) was added 1M THF (3 ml) solution of tetrabutylammonium fluoride. After being stirred for 1 hour at room temperature, the mixture was partitioned between ethyl acetate and sat. NaHCO3. The organic layer was washed with brine. The dried solvent was evaporated in vacuo. The residue was purified by chromatography on silica gel to give 2-[(4,5-diphenyloxazol-2-yl)methylamino]-1,2,3,4-tetrahydro-5-hydroxynaphthalene (0.66 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-92d04d8b15ad4d03ba23a33bd031cca8 |
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| Source note | uspto-grants-2001_10 |
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