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HRID 429402作成日:2026年10月25日

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

https://huagongshe.com/reaction/429402

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US06316496B1
出典データセットuspto-grants-2001_11
ORD IDord-c33a48a3d78b4f6ca7c7bed3db66c2b4
出典メモuspto-grants-2001_11