HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268701Generated: October 30, 2026
Potassium Carbonate → Tert-butyl-7-[(2-(4-bromophenyl)-5-methyl-1,3-oxazol-4-yl)methoxy]chromane-3-carboxylate
https://huagongshe.com/reaction/268701
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(4-Bromophenyl)-4-(chloromethyl)-5-methyloxazole | HCID 10957108 | — |
| Reactant | Tert-butyl 7-hydroxychromane-3-carboxylate | HCID 59832111 | — |
| Solvent | Water | HCID 962 | — |
| Product | Tert-butyl-7-[(2-(4-bromophenyl)-5-methyl-1,3-oxazol-4-yl)methoxy]chromane-3-carboxylate | HCID 69279608 | 77.4% |
Reaction Steps
To a stirred suspension of tert-butyl 7-hydroxychromane-3-carboxylate (1.1 g, 4.4 mmol) and potassium carbonate (1.1 g, 8 mmol), 2-(4-bromophenyl)-4-(chloromethyl)-5-methyl-1,3-oxazole (1.14 g, 4 mmol) was added and the reaction mixture was stirred at 60° C. for overnight. After the completion of the reaction, water (40 ml) was added and the precipitated product was extracted with ethylacetate (60 ml). The organic layer was washed with 50 ml of water twice and dried. The dried solution was evaporated to give the product as brown solid (1.55 g, 77.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07446127B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-a3d340ab3ed64250b45df0e7cea8363c |
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| Source note | uspto-grants-2008_11 |
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