HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355417Generated: October 26, 2026
Phosphorus oxychloride → 10-Ethylphenothiazine-3-carbaldehyde
https://huagongshe.com/reaction/355417
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | N-Methylformanilide | HCID 66737 | — |
| Reactant | N-Ethylphenothiazine | HCID 219178 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | 1,2-Dichlorobenzene | HCID 7239 | — |
| Product | 10-Ethylphenothiazine-3-carbaldehyde | HCID 314330 | 69% |
Reaction Steps
N-Methylformanilide (5.35 ml, 43.6 mmol) and phosphorus oxychloride (4.06 ml, 43.6 mmol) were added at room temperature to a mixture of 10-ethylphenothiazine (7.62 g, 33.5 mmol) and 1,2-dichlorobenzene (34 ml), and the mixture was stirred at 100° C. for 24 hours. At room temperature, a sodium acetate aqueous solution (45 wt. %, 85 g) was added to the reaction mixture, which was subsequently concentrated under a reduced pressure. Ethyl acetate and water (each 300 ml) were added to the resulting residue in that order and then the reaction product was extracted with ethyl acetate. 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; hexane:ethyl acetate=5:1) to give the title compound (5.91 g, 23.1 mmol, 69%) 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-1437272821134a61a16b6222de15954f |
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| Source note | uspto-grants-1998_11 |
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