HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15417Generated: October 29, 2026
p-Toluenesulfonic acid → Methyl 3-[5-(hydroxymethyl)-imidazol-1-yl]-3-(4-cyano-phenyl)-propionate
https://huagongshe.com/reaction/15417
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Methyl 3-[5-(t-butyl-dimethylsilanyloxymethyl)-imidazole-1-yl]-3-(4-cyanophenyl)-propionate | HCID 68695105 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 3-[5-(hydroxymethyl)-imidazol-1-yl]-3-(4-cyano-phenyl)-propionate | HCID 17975627 | — |
Reaction Steps
The title A compound, methyl 3-[5-(t-butyl-dimethylsilanyloxymethyl)-imidazole-1-yl]-3-(4-cyanophenyl)-propionate (0.98 g, 2.46 mmol) and p-toluenesulfonic acid (0.55 g, 2.9 mmol) are stirred in MeOH (10 mL) at RT for 24 h. The reaction mixture is evaporated to an oil and partitioned between EtOAc and aqueous saturated sodium bicarbonate. The combined organic phases are dried over anhydrous sodium sulfate and removal of the solvent in vacuo yields methyl 3-[5-(hydroxymethyl)-imidazol-1-yl]-3-(4-cyano-phenyl)-propionate as an oil: 1H-NMR (CDCl3) δ 7.65 (2H, d, J=8.4), 7.62 (1H, s), 7.31 (2H, d, J=8.4), 6.98 (1H, s), 6.05 (1H, dd, J=9.2, 6.2), 4.62 (1H, d, J=13.5), 4.47 (1H, d, J=13.5), 3.67 (3H, s), 3.36 (1H, dd, J=16.5, 9.2), 3.21 (1H, dd, J=16.5, 6.2); e/z (ES) 286 (M+1, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07732603B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-19f1badb0526496eb7446ade120ca37b |
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| Source note | uspto-grants-2010_06 |
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