HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 45201Erstellt: 24. Oktober 2026
Sodium Hydroxide → 1-(1,4-Dioxa-spiro[4.5]dec-8-yl)-1-phenyl-ethylamine
https://huagongshe.com/de/reaction/45201
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 1,4-Dioxaspiro[4.5]decane-8-carbonitrile | HCID 11116433 | — |
| Edukt | HCID 178418255 | HCID 178418255 | — |
| Edukt | HCID 178418348 | HCID 178418348 | — |
| Katalysator | Titanium isopropoxide | HCID 11026 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | 1-(1,4-Dioxa-spiro[4.5]dec-8-yl)-1-phenyl-ethylamine | HCID 58381015 | — |
Reaktionsschritte
Under argon, phenylmagnesium bromide (3M) in diethyl ether (6.7 mL, 20 mmol) was added to a solution of 1,4-dioxa-spiro[4.5]decane-8-carbonitrile (3.34 g, 20 mmol) in diethyl ether (60 mL). The mixture was stirred for 30 minutes. Titanium (IV) isopropoxide (5.7 g, 20 mmol) was then added. After stirring for 5 min, methyl lithium (1.6 M in diethyl ether, 31.2 mL, 50 mmol) was added and the reaction was heated under reflux for 10 hours. After cooling in ice/water the brown mixture was treated cautiously with 2M NaOH solution (30 mL) dropwise (exothermic). The mixture was extracted with t-butyl methyl ether and dried over sodium sulphate. After filtration the organic phase was evaporated to give 5 g of a pale yellow oil, which was used in the next step without further purification. Rt=2.10 min (Method 2). Detected mass: 261.2 (M+H+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08541449B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-7306a45cd4c24805a47794cf7597b8ed |
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| Quellennotiz | uspto-grants-2013_09 |
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