HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355422Generated: October 29, 2026
Dichloromethane → HCID 15425737, compound
https://huagongshe.com/reaction/355422
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 10-Methyl-10H-phenothiazine-3-carbaldehyde | HCID 617826 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 15425737 | HCID 15425737 | 63.4% |
Reaction Steps
In an atmosphere of argon, carbon tetrabromide (8.29 g, 25 mmol) and zinc powder (1.63 g, 25 mmol) were added in that order to a mixture of triphenylphosphine (6.56 g, 25 mmol) and dichloromethane (75 ml), and the mixture was stirred at room temperature for 23 hours. A dichloromethane (25 ml) solution of 3-formyl-10-methylphenothiazine (3.02 g, 12.5 mmol) was added and the mixture was again stirred for 7 hours. The reaction mixture was diluted with hexane and the insoluble matter was removed by filtration. The reaction product was extracted from the insoluble matter three times with hexane (about 60° C.), and the thus collected organic layers were combined and concentrated under a reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent; ethyl acetate:dichloromethane:hexane=10:10:80) to give the title compound (3.15 g, 7.93 mmol, 63%) as yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05830902 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-ef7750ff920b464aa4fa1afbc4bc118d |
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| Source note | uspto-grants-1998_11 |
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