HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 249165Erstellt: 25. Oktober 2026
Phenothiazine → Tert-butyl 3-(phenothiazin-10-ylmethyl)benzoate
https://huagongshe.com/reaction/249165
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Phenothiazine | HCID 7108 | — |
| Edukt | Methyl 3-(chloromethyl)benzoate | HCID 3248988 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Tert-butyl 3-(phenothiazin-10-ylmethyl)benzoate | HCID 19024810 | 30,6% |
Reaktionsschritte
To a solution of phenothiazine (1.00 g) in tetrahydrofuran (10 ml) was added potassium tert-butoxide (617 mg) at 0° C. The mixture was stirred at 0° C. for 20 minutes, and then a solution of methyl 3-(chloromethyl)benzoate (1.02 g) in tetrahydrofuran (10 ml) was added. The mixture was stirred at 25° C. for 3 hours, and then potassium tert-butoxide (1.02 g) was added. The mixture was stirred at 25° C. for 1 hour, and then evaporated. The residue was partitioned between ethyl acetate and 0.1N hydrochloric acid. The organic layer was washed with water and brine, dried over magnesium sulfate, and evaporated. The residue was chromatographed on silica gel eluting with a mixture of hexane and ethyl acetate (40:1) to give tert-butyl 3-(phenothiazin-10-ylmethyl)benzoate (598 mg) as crystals.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05212320 |
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| Quelldatensatz | uspto-grants-1993_05 |
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| ORD ID | ord-5de86612323143d4aaac4815ed542123 |
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| Quellennotiz | uspto-grants-1993_05 |
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