HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1252217Erstellt: 27. Oktober 2026
4-Nitrobenzyl alcohol → p-Nitrobenzyl 4-p-methoxybenzyloxycarbonyl-4-methylvalerate
https://huagongshe.com/reaction/1252217
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Nitrobenzyl alcohol | HCID 69275 | — |
| Edukt | 4-Methyloxybenzyl chloride | HCID 69993 | — |
| Edukt | Dihydro-3,3-dimethyl-2H-pyran-2,6(3H)-dione | HCID 76247 | — |
| Edukt | p-Nitrobenzyl 4-carboxy-4-methylvalerate | HCID 20140795 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | p-Nitrobenzyl 4-p-methoxybenzyloxycarbonyl-4-methylvalerate | HCID 20140840 | — |
Reaktionsschritte
To a solution of p-nitrobenzyl 4-carboxy-4-methylvalerate (17.26 g) in dry dimethylformamide (100 ml), prepared by the procedure similar to that described in Example 174 from 2,2-dimethylglutaric anhydride and p-nitrobenzyl alcohol, was added p-methoxybenzyl chloride (9.16 g) and triethylamine (5.91 g). The reaction mixture was stirred at 80° C. for 9.5 hours, diluted with water and extracted with diethyl ether. The extract was washed successively with aqueous potassium carbonate, water, dilute hydrochloric acid and again water, dried over anhydrous sodium sulfate and evaporated to give p-nitrobenzyl 4-p-methoxybenzyloxycarbonyl-4-methylvalerate.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04742052 |
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| Quelldatensatz | uspto-grants-1988_05 |
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| ORD ID | ord-2bae3c7b3497440ab93648332a424e42 |
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| Quellennotiz | uspto-grants-1988_05 |
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