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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934479Generated: November 1, 2026

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

https://huagongshe.com/reaction/1934479

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 min. and at room temperature for 3 hr. The resulting dark colored reaction mixture was carefully poured into an ice-water mixture (200 mL) and stirred at room temperature for 30 min. The resulting precipitate was filtered and washed throughly with cold water (500 ml). The solid was dried overnight under high vacuum in a desiccator over NaOH pallets to yield the desired compound (5.9 g. 78%) as a grey powder. 1H NMR (DMSO-d6) 3.89 (s, 3H), 7.55 (d, 1H, J=8.4 Hz.) 7.65 (d, 1H, J=8.4 Hz), 7.88 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384036B1
Source datasetuspto-grants-2002_05
ORD IDord-436d62d0dfdc48cf99457d392fd4214a
Source noteuspto-grants-2002_05