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HRID 11252作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Chlorosulfonic acidHCID 24638—
反応物CarbendazimHCID 25429—
生成物Methyl N-[6-(chlorosulfonyl)-1H-benzimidazol-2-yl]carbamateHCID 1512404778%

反応手順

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)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07098202B2
出典データセットuspto-grants-2006_08
ORD IDord-ec436e219a7b4e779e97414f5d0737fc
出典メモuspto-grants-2006_08