Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Einecs 211-027-4 | HCID 69401 | — |
| Reactant | Methyl phenothiazin-2-yl ether | HCID 74490 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 10H-phenothiazin-2-ol | HCID 10608713 | 53% |
Reaction Steps
A mixture of 25 g (109 mmol) of 2-methoxyphenothiazine and 60 g (4.8 eq.) of pyridinium chloride is heated at 170° C. for 15 hours. After cooling down to a temperature of approximately 80° C., the brown solution obtained is diluted with 200 ml of ethyl acetate. Stirring is maintained for 30 minutes before pouring the reaction mixture into 200 ml of water. After stirring and decantation, the organic phase is dried over sodium sulphate and concentrated to dryness, under vacuum. The greenish solid obtained is recrystallized from 700 ml of boiling toluene. An insoluble solid is eliminated by filtration, the filtrate crystallizes spontaneously overnight. The crystals are collected by filtration and rinsed using isopentane. After drying, 12.43 g of a grey solid is obtained with a yield of 53%. Melting point: 207-208° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07384933B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-bfda4e5cfadb4994b4f0898525785a7d |
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| Source note | uspto-grants-2008_06 |
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