HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395161Generated: November 1, 2026
Diethyl Ether → 4-Diethoxymethyl-10-methyl-phenothiazine
https://huagongshe.com/reaction/2395161
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 10-Methylphenothiazine-4-carbaldehyde | HCID 3812154 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Diethoxymethyl-10-methyl-phenothiazine | HCID 18972515 | 96.2% |
Reaction Steps
15.0 ml of triethyl orthoformate were added at room temperature to a solution of 4.90 g (20.3 mmol) of 10-methyl-phenothiazine-4-carbaldehyde and 50 mg of p-toluenesulphonic aci×1H2O in 15 ml of methanol. The reaction mixture was boiled at reflux for 45 minutes, cooled and poured into 30 g of ice, 30 ml of saturated aqueous sodium hydrogen carbonate solution and 100 ml of diethyl ether. The organic phase was washed with 50 ml of saturated sodium chloride solution, dried over magnesium sulphate and concentrated. The residue was chromatographed on 300 g of silica gel with diethyl ether/hexane (1:4), whereupon, after crystallization from diethyl ether/hexane in a refrigerator, 6.16 g (96.2%) of 4-diethoxymethyl-10-methyl-phenothiazine were obtained as a white solid of m.p. 44.6°-46.2°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05811548 |
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| Source dataset | uspto-grants-1998_09 |
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| ORD ID | ord-1dd7eebba0b94059bb2fc44ff392bb7e |
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| Source note | uspto-grants-1998_09 |
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