HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636039Generated: October 29, 2026
Methanesulfonic Acid → HCID 22475896, compound
https://huagongshe.com/reaction/1636039
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | 3-Mercaptopropionic Acid | HCID 6514 | — |
| Reactant | Diphenyl Ether | HCID 7583 | — |
| Reactant | 2,7Dibromofluorenone | HCID 53420103 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 22475896 | HCID 22475896 | — |
Reaction Steps
To a stirred mixture of 2,7-dibromofluorenone (26 g, 77 mmoles) and phenyl ether (170 g, 1 mole) is added 60 mL of methanesulfonic acid and 0.5 mL of 3-mercaptopropionic acid. The mixture is heated and stirred at 60° C. for 30 minutes, and then at 25° C. for 16 hours. The mixture is again stirred at 60° C. for 30 minutes and then at 25° C. for 3 hours. The mixture is poured into 1.4 L of ice water and 200 mL of methanol and allowed to stand in the hood for 4 days. The semi-solid precipitate is separated by decanting the supernatant liquid and then digesting with 1:1 v/v acetonitrile-hexane. The title compound is obtained as a colorless powder (32 g, 64 percent), melting point 178° C. to 180° C. HPLC analysis shows a purity of greater than 99 percent and the PMR spectrum (DMSO-d6) is consistent with the structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06512083B1 |
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| Source dataset | uspto-grants-2003_01 |
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| ORD ID | ord-7f0d61b723a84eb0bcdb0fe179b0d6ee |
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| Source note | uspto-grants-2003_01 |
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