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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 11252Erstellt: 23. Oktober 2026

Chlorosulfonic acid → Methyl N-[6-(chlorosulfonyl)-1H-benzimidazol-2-yl]carbamate

https://huagongshe.com/de/reaction/11252

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChlorosulfonic acidHCID 24638—
EduktCarbendazimHCID 25429—
ProduktMethyl N-[6-(chlorosulfonyl)-1H-benzimidazol-2-yl]carbamateHCID 1512404778%

Reaktionsschritte

A solution of 2-carbomethoxyamino-benzimidazole (5.0 g, 0.026 mole) in chlorosulfonic acid (35.00 mL) was stirred at 0° C. for 30 minutes and at room temperature for 3 hours. The resulting dark colored reaction mixture was poured into an ice-water mixture (200 mL), and stirred at room temperature for 30 minutes. The resulting precipitate was filtered and washed with cold water (500 mL). The solid was dried overnight under high vacuum in a desiccator over NaOH pellets to give 5-chlorosulfonyl-2-carbomethoxyamino-benzimidazole (5.9 g, 78%) as a grey powder. 1H NMR DMSO-d6) d: 3.89 (s, 3H), 7.55 (d, J=8.4 Hz, 1H), 7.65 (d, J=8.4 Hz, 1H), 7.88 (s, 1H). (German Patent DE 3826036)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07098202B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-ec436e219a7b4e779e97414f5d0737fc
Quellennotizuspto-grants-2006_08