HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 2-(3-(4-Benzyloxybenzyl)-2-oxoimidazolidin-1-yl)-3-methylbutyric acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 2-(3-(4-benzyloxybenzyl)-2-oxoimidazolidin-1-yl)-3-methylbutyrate | HCID 68538627 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(3-(4-Benzyloxybenzyl)-2-oxoimidazolidin-1-yl)-3-methylbutyric acid | HCID 68539058 | 82.5% |
Reaction Steps
Ethyl 2-(3-(4-benzyloxybenzyl)-2-oxoimidazolidin-1-yl)-3-methylbutyrate (0.330 g; 0.80 mmol) was dissolved in methanol (MeOH; 6 ml). NaOH solution (1N; 3 ml) as added, and the mixture was stirred at RT for 3 h. The solvent was removed under reduced pressure, and saturated NaH2PO4 solution (2 ml) was added to he residue. The solid was filtered off with suction and dried under reduced pressure at 60° C. to result in 2-(3-(4-benzyloxybenzyl)-2-oxoimidazolidin-1-yl)-3-methylbutyric acid (0.25 g; 0.66 mmol). MS: 383.10 (M+H); Rt: 1.57 min (method: gradient 0 min 90% H2O (0.05% TFA) 1.9 min 95% acetonitrile, 95% acetonitrile to 2.4 min, 10% acetonitrile 2.45 min; flow rate 1 ml/min; column 0.4 μL (YMC J'sphere ODS H80 20X2 1.4μ); 30° C.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07652143B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-ac34fca295c3412cabff067fa2c05935 |
| Source note | uspto-grants-2010_01 |