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HRID 429402생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/429402

반응식

참여 물질

역할이름HCID투입량
반응물Chlorosulfonic acidHCID 24638—
반응물CarbendazimHCID 25429—
생성물Methyl N-[6-(chlorosulfonyl)-1H-benzimidazol-2-yl]carbamateHCID 1512404778%

반응 단계

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)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06316496B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-c33a48a3d78b4f6ca7c7bed3db66c2b4
출처 메모uspto-grants-2001_11