HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2294765Erstellt: 25. Oktober 2026
4-Toluenesulfonyl chloride → 1,3-Di-tert-butyl 2-diazopropanedioate
https://huagongshe.com/reaction/2294765
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Sodium Azide | HCID 33557 | — |
| Edukt | Di-tert-butyl malonate | HCID 68324 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 1,3-Di-tert-butyl 2-diazopropanedioate | HCID 5014600 | 125,9% |
Reaktionsschritte
A mixture of sodium azide (1.37 grams, 21.0 mmol), p-toluenesulfonyl chloride (4.0 grams, 21.0 mmol), and 70% aqueous ethanol (60 mL) was stirred at room temperature for 1 hour. Di-t-butyl malonate (4.48 mL, 20.0 mmol) and triethylamine (2.92 grams, 21.0 mmol) were added. The reaction mixture was stirred at room temperature for 4 hours and then poured into deionized water (200 mL). The mixture was extracted with petroleum ether (2×200 mL). The extracts were combined and then washed with a saturated aqueous sodium chloride solution. The organic solution was dried using anhydrous magnesium sulfate, filtered, and concentrated to give 6.10 grams of di-t-butyl-2-diazomalonate as a yellow oil. IR(film): 2110 cm-1. Decomposition temperature: 178° C. (by DSC).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05691098 |
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| Quelldatensatz | uspto-grants-1997_11 |
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| ORD ID | ord-a7509a42deed4107a58581aeb696dc14 |
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| Quellennotiz | uspto-grants-1997_11 |
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