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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247905Generated: November 1, 2026

p-Toluenesulfonic acid → HCID 54543058, compound

https://huagongshe.com/reaction/2247905

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 54045049HCID 54045049—
SolventEthanolHCID 702—
ProductHCID 54543058HCID 5454305846%

Reaction Steps

A solution of 10.5 parts of intermediate 60, namely ethyl [4-[(1H-imidazol-1-yl)phenylmethyl]-2-[[(tetrahydro-2H-pyran-2-yl)oxy]methyl]phenyl]carbamate, 5.5 parts of 4-methylbenzenesulfonic acid and 198 parts of ethanol was stirred over weekend at room temperature and for a short time at 50°-60° C. After cooling, there were added ethanol and Na2CO3. The whole was stirred for 15 min. and was then filtered. The filtrate was evaporated and the residue was partitioned between dichloromethane and water. The organic layer was separated and the aqueous layer was re-extracted with dichloromethane. The combined dichloromethane layers were dried, filtered and evaporated. The residue was purified by column chromatography (silica gel; CHCl3 /CH3OH 95:5). The eluent of the desired fraction was evaporated and the residue was co-evaporated with methylbenzene. The crystallized product was filtered off, stirred in 2,2'-oxybispropane and dried in vacuo, yielding 4.65 parts (46.0%) of ethyl [2-(hydroxymethyl)-4-[(1H-imidazol-1-yl)phenylmethyl]phenyl]carbamate; mp. 143.1° C. (interm. 61).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05037829
Source datasetuspto-grants-1991_08
ORD IDord-9c69862fafff4ac2adddbde28167a9e3
Source noteuspto-grants-1991_08