HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874604Generated: October 27, 2026
Trimethyl orthoformate → 6-Bromo-5-chlorobenzoxazole
https://huagongshe.com/reaction/874604
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | Ytterbium triflate | HCID 2733225 | — |
| Reactant | 2-Amino-5-bromo-4-chlorophenol | HCID 58487100 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 6-Bromo-5-chlorobenzoxazole | HCID 58487277 | 6,559.2% |
Reaction Steps
A mixture of 2-amino-5-bromo-4-chlorophenol (29) (865 mg, 3.89 mmol), trifluoromethanesulfonic acid Ytterbium (III) salt (24 mg, 1% mol) and trimethyl orthoformate (511 μl, 1.2 eq.) in 2 ml EtOH was heated at 90° C. for 2 h. After cooling down to r.t., the reaction mixture was taken up in EA, washed with aq. NaHCO3 and brine, dried over Na2SO4, concentrated to dryness. The resulting brown solid was dissolved in DCM and subjected to silica gel column purification using 0-100% B (A: hexane; B: 50% EA in hexane) to furnish 590 mg 30 as yellow solid (yield: 65.2%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08980629B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-2c55f35bb8d9410eabf22e12ba737ad9 |
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| Source note | uspto-grants-2015_03 |
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