HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 40306Erstellt: 25. Oktober 2026
2-Methoxyethanol → Tert-butyl 2-(3-(2-methoxyethoxy)quinolin-6-yl)acetate
https://huagongshe.com/reaction/40306
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Methoxyethanol | HCID 8019 | — |
| Edukt | Tributylphosphine | HCID 13831 | — |
| Edukt | Methoxymethanol | HCID 62540 | — |
| Edukt | 1,1'-(Azodicarbonyl)dipiperidine | HCID 73042 | — |
| Edukt | Tert-butyl 2-(3-hydroxyquinolin-6-yl)acetate | HCID 57691372 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Lösungsmittel | Hexane | HCID 8058 | — |
| Produkt | Tert-butyl 2-(3-(2-methoxyethoxy)quinolin-6-yl)acetate | HCID 57690925 | — |
Reaktionsschritte
To a suspension of tert-butyl 2-(3-hydroxyquinolin-6-yl)acetate (0.1 g, 0.4 mmol) in benzene (5 mL) was added 2-methoxyethanol (0.09 ml, 1 mmol) and tri-n-butylphosphine (0.1 ml, 0.6 mmol). The resulting mixture was cooled to 0° C. followed by adding 1.1′-(azodicarbonyl)dipiperidine (0.1 g, 0.6 mmol). After 10 min, ice bath was removed; the reaction mixture was warmed up to rt. After 2 h, TLC showed there still existed 50% starting material. More methoxymethanol (2 eq, 0.06 mL) was added. The reaction mixture was continued to stir for 20 h. Hexane was added to the reaction mixture and dihydro-ADDP separated out was filtered off. The filtrate was concentrated. The crude product was purified using SiO2 chromatography (Teledyne Isco RediSep®, P/N 68-2203-027, 40 g SiO2, hexane:acetone=85%:15%, Flow=40 mL/min) to afford the desired product as colorless liquid. MS m/z: 318.4 (M+H). Calc'd. for C18H23NO4—317.38.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08524900B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-8b3c19f1206044a083f5bf503bf64eb7 |
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| Quellennotiz | uspto-grants-2013_09 |
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