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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Toluenesulfonyl chlorideHCID 7397—
EduktTriethylamineHCID 8471—
EduktSodium AzideHCID 33557—
EduktDi-tert-butyl malonateHCID 68324—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
Produkt1,3-Di-tert-butyl 2-diazopropanedioateHCID 5014600125,9%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05691098
Quelldatensatzuspto-grants-1997_11
ORD IDord-a7509a42deed4107a58581aeb696dc14
Quellennotizuspto-grants-1997_11