HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 581209Generated: October 25, 2026
8-Methoxypsoralen → 4-Bromo-9-methoxy-7h-furo[3,2-g]chromen-7-one
https://huagongshe.com/reaction/581209
Participants
| Role | Name | HCID | Charge |
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| Reactant | 8-Methoxypsoralen | HCID 4114 | — |
| Reactant | Bromine | HCID 24408 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Bromo-9-methoxy-7h-furo[3,2-g]chromen-7-one | HCID 240048 | 91.2% |
Reaction Steps
8-methoxypsoralen (4.32 g, 20.0 mmol), obtained from Aldrich Chemical Company was dissolved in tetrahydrofuran (50 mL). To the mixture was added dropwise, with stirring, elemental bromine (4.0 g, 25 mmol) over 20 min at room temperature. The reaction mixture turned red when bromine was added. Precipitate appeared in 5 min. Extra bromine was consumed by solvent tetrahydrofuran in an extended 2 hr stirring or by the addition of 10% sodium thiosulfate solution. The crude product was collected by filtration and was purified with recrystallization from ethanol to give the product 5-bromo-8-methoxypsoralen (5.38 g, 91% yield) as a white solid. mp 178-80° C. 1H--NMR (DMSO(dimethylsulfoxide)--d6, ppm): 8.22(d, J=2.2 Hz, 1H), 8.11 (d, J=9.9 Hz, 1H),7.01(d,J=2.2 Hz, 1H),6.53(d, J=9.9 Hz, 1H),4.17(s,3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05919935 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-a583aa25c2164dd0916f6b0636124b53 |
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| Source note | uspto-grants-1999_07 |
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