HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1578236Erstellt: 27. Oktober 2026
Phenothiazine → N-(2-acryloxyethyl)-2,2,4-trimethyldecahydroquinoline
https://huagongshe.com/reaction/1578236
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Phenothiazine | HCID 7108 | — |
| Edukt | Methyl Acrylate | HCID 7294 | — |
| Edukt | 1-(2-Hydroxyethyl)-2,2,4-triethyldecahydroquinoline | HCID 20568281 | — |
| Katalysator | Zinc Carbonate | HCID 19005 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | N-(2-acryloxyethyl)-2,2,4-trimethyldecahydroquinoline | HCID 20568277 | — |
Reaktionsschritte
Following the method described in U.S. Pat. No. 3,872,161, the title compound was prepared by reacting 1 mole of 1-(2-hydroxyethyl)-2,2,4-triethyldecahydroquinoline (hereinafter referred to as HETDQ) with 3 moles methylacrylate in the presence of 0.8 gram phenothiazine and 13 grams zinc carbonate. The above mixture was heated to 87° C. in a 1 liter 3-necked flask equipped with a fractionating column. The pot temperature was gradually increased to a maximum of 164° C. while methanol and other lower boiling point liquid fractions were collected. The reaction took four days.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04292237 |
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| Quelldatensatz | uspto-grants-1981_09 |
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| ORD ID | ord-cb8d79e5dd1542a5aac1341e9ec57eef |
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| Quellennotiz | uspto-grants-1981_09 |
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