HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828827Generated: November 1, 2026
p-Toluenesulfonyl isocyanate → HCID 22058622, compound
https://huagongshe.com/reaction/1828827
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Toluenesulfonyl isocyanate | HCID 77703 | — |
| Reactant | HCID 22058647 | HCID 22058647 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 22058622 | HCID 22058622 | 75.6% |
Reaction Steps
4-Chloro-1-(2-chloro-4-(1-pentyloxy)benzyl)-5-hydroxymethyl-2-methyl-1H-imidazole (150 mg) was dissolved in 1,4-dioxane (1.5 ml) and p-toluenesulfonyl isocyanate (99 mg) was added at room temperature. The reaction mixture was stirred at room temperature for 1 hr and concentrated under reduced pressure. To the residue was added ethanol (5 ml) and the precipitated crystals were collected by filtration. The crystals were dissolved in ethyl acetate (2 ml), and hexane (13 ml) was added on an oil bath at 70° C. The mixture was allowed to cool and the precipitated crystals were collected by filtration. The crystals were dried by heating under reduced pressure to give (4-chloro-1-(2-chloro-4-(1-pentyloxy)benzyl)-2-methyl-1H-imidazol-5-yl)methyl N-(4-methylbenzenesulfonyl)carbamate (176 mg) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07060721B1 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-1c0a7e62692e409cb80118b054fb085e |
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| Source note | uspto-grants-2006_06 |
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