HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037371Generated: November 3, 2026
Boron tribromide → 7-Amino-8-hydroxy-3-iodo-2-phenyl-chromen-4-one
https://huagongshe.com/reaction/1037371
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 7-Amino-3-iodo-8-methoxy-2-phenyl-chromen-4-one | HCID 67067790 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-Amino-8-hydroxy-3-iodo-2-phenyl-chromen-4-one | HCID 67067919 | 85% |
Reaction Steps
To a solution of 7-amino-3-iodo-8-methoxy-2-phenyl-chromen-4-one (494 mg, 1.26 mmol) in DCM (25 mL) under a nitrogen atmosphere at −78° C. was added a solution of BBr3 (1 M in DCM, 8 mL, 8 mmol) dropwise over 15 mins. The mixture was stirred at −78° C. for 1 hour before allowing to warm to RT and stirred for a further 18 hours. The reaction mixture was quenched with the slow addition of saturated aqueous NaHCO3. DCM was added and the resulting biphasic mixture was separated. The aqueous layer was extracted with DCM (2×50 mL) and the combined organic phase was washed with brine, dried (NaSO4), filtered, and the solvent removed to give the title compound as a brown solid (405 mg, 85%). LCMS (Method G): RT=3.04 min, [M+H]+=380.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546376B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-7193569dd6974b5caff581f3a341131f |
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| Source note | uspto-grants-2013_10 |
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