HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 56766Erstellt: 24. Oktober 2026
Ammonium Chloride → Tert-butyl 2-(2-methoxyethyl)-1,3-dithiane-2-carboxylate
https://huagongshe.com/de/reaction/56766
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | 1-Iodo-2-methoxyethane | HCID 79136 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Edukt | Tert-butyl 1,3-dithiane-2-carboxylate | HCID 86007917 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Tert-butyl 2-(2-methoxyethyl)-1,3-dithiane-2-carboxylate | HCID 90060334 | — |
Reaktionsschritte
10.2 g (46.1 mmol) of tert-butyl 1,3-dithiane-2-carboxylate and 12.0 g (64.5 mmol) of 1-iodo-2-methoxyethane were initially charged in 127 ml of dimethylformamide, the mixture was cooled to 0° C. and 6.21 g (55.3 mmol) of potassium tert-butoxide were added. The resulting reaction mixture was stirred at 0° C. for 1 h and at RT for 16 h. The reaction mixture was added to 1.5 l of a 1:2 mixture of ice and saturated aqueous ammonium chloride solution and extracted three times with 300 ml of diethyl ether. The combined organic phases were dried over magnesium sulphate and filtered, and the solvent was removed under reduced pressure. The crude product was used for the next step without further purification. Yield: 11.1 g (87% of theory)
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09434690B2 |
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| Quelldatensatz | uspto-grants-2016_09 |
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| ORD ID | ord-23e59bb0f1e44d93a51a2c618ff37b6d |
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| Quellennotiz | uspto-grants-2016_09 |
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