HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → HCID 11482338, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 10H-phenothiazine-3-methanol, 10-methyl- | HCID 638533 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 11482338 | HCID 11482338 | 94% |
Reaction Steps
With ice-cooling, m-chloroperbenzoic acid (1.66 g, 9.6 mmol) was added to a mixture of 3-hydroxymethyl-10-methylphenothiazine (1.94 g, 8.0 mmol) and dichloromethane (30 ml), and the mixture was stirred for 1.5 hours and then at room temperature for 1.5 hours. A saturated sodium bicarbonate aqueous solution was added to the reaction mixture and the reaction product was extracted with chloroform. The extract was dried over anhydrous magnesium sulfate and then concentrated under a reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent; methanol:chloroform=3:97 then 10:90) to give the title compound (1.95 g, 7.52 mmol, 94%) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05830902 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-7d01e06b8cdb42789781689c819db878 |
| Source note | uspto-grants-1998_11 |