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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494048Generated: October 30, 2026

Benzyl Alcohol → Sulfamic acid 4-(2-methyl-1H-imidazol-1-yl)phenyl ester monohydrochloride

https://huagongshe.com/reaction/1494048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantIsopropanolHCID 3776—
ReactantChlorosulfonyl isocyanateHCID 70918—
Reactant4-(2-Methyl-1H-imidazol-1-YL)phenolHCID 11252289—
ReactantEthyl acetate methanol ammonium hydroxideHCID 21901312—
SolventAcetonitrileHCID 6342—
ProductSulfamic acid 4-(2-methyl-1H-imidazol-1-yl)phenyl ester monohydrochlorideHCID 67854696—

Reaction Steps

To a chilled solution of acetonitrile (50 ml) and chlorosulfonyl isocyanate (12.16 g, 0.086 mole) was added benzyl alcohol (9.29 g, 0.086 mole) while maintaining the temperature between 10°-15° C. The reaction stirred at room temperature 1.5 hr and 4-(2-methyl-1H-imidazol-1-yl)phenol (10.0 g, 0.057 mole) added in small portions) while maintaining the temperature below 20° C. The reaction was stirred overnight and its progress checked by thin layer chromatography (8:1:1 ethyl acetate/methanol/ammonium hydroxide). Once the reaction had gone to completion, isopropyl alcohol (3.42 g, 0.057 mole) was added and reaction stirred an additional hour. The solution was concentrated and the residue dissolved in methanol (150 ml) and the solution subjected to catalytic hydrogenation using 5% palladium on carbon catalyst. The solution was filtered and the filtrate concentrated, replacing the methanol with isopropyl alcohol. White crystals precipitated and were collected and dried (9.8 g, 59.5%, mp 197°-200° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05025031
Source datasetuspto-grants-1991_06
ORD IDord-63c86531ecdc4795ac793cd6454ebda5
Source noteuspto-grants-1991_06