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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323754Generated: October 26, 2026

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

https://huagongshe.com/reaction/323754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonic acidHCID 24638—
ReactantCarbendazimHCID 25429—
ProductMethyl N-[6-(chlorosulfonyl)-1H-benzimidazol-2-yl]carbamateHCID 1512404778%

Reaction Steps

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)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06214861B1
Source datasetuspto-grants-2001_04
ORD IDord-1722a476cb3f4a10ad70b47b999e07fe
Source noteuspto-grants-2001_04