HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247905Generated: November 1, 2026
p-Toluenesulfonic acid → HCID 54543058, compound
https://huagongshe.com/reaction/2247905
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 54045049 | HCID 54045049 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 54543058 | HCID 54543058 | 46% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05037829 |
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| Source dataset | uspto-grants-1991_08 |
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| ORD ID | ord-9c69862fafff4ac2adddbde28167a9e3 |
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| Source note | uspto-grants-1991_08 |
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