HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475146Generated: October 29, 2026
p-Toluenesulfonic acid → HCID 86694705, compound
https://huagongshe.com/reaction/475146
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | HCID 71272278 | HCID 71272278 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86694705 | HCID 86694705 | 99.8% |
Reaction Steps
A mixture of 1-(6-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-benzo[d]imidazol-4-yl)ethanone (1.0 g, 3.82 mmol) and TsOH (1.97 g, 11.45 mmol) in water (10 mL) and MeOH (50 mL) was heated at 80° C. for 3 h. The reaction mixture was quenched with EtOAc (50 mL) and water (50 mL). The aqueous phase was extracted with EtOAc (50 mL×2). The combined organic layers were washed with water and brine, dried (Na2SO4), filtered, and concentrated in vacuo to afford 1-(6-fluoro-1H-benzo[d]imidazol-4-yl)ethanone as a yellow solid (678 mg, 99.8%). MS (ESI): m/z=179.3 [M+1].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08637537B2 |
|---|
| Source dataset | uspto-grants-2014_01 |
|---|
| ORD ID | ord-1fe6d9deaa5e49178199aa0f2c65f3f3 |
|---|
| Source note | uspto-grants-2014_01 |
|---|