Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 57443412 | HCID 57443412 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11278150 | HCID 11278150 | 78% |
Reaction Steps
10.8 mg of LiOHH2O solution (0.25 mM) was added to 0.86 ml of THF solution containing 55 mg of 3-[1-(2,4-dimethoxy benzyl)-2-oxo-2,5-dihydro-1H-pyrrol-3-yl]-propionic acid methyl ester (0.17 mM) in a dropwise manner at 0° C. The reaction mixture was stirred for 2 hrs at 0° C. adjust pH 1 with 5% HCl was added to the mixture to pH 1. Then the mixture was extracted three times with 10 ml of ethyl acetate, the organic layer was washed with 15 ml of saturated NaCl solution, dried over anhydrous MgSO4, filtered and concentrated in vacuo. The resulting compound was purified with Silica gel column chromatography with a solvent mixture mixed with methanol and chloroform (1:9) as an eluant to give 41 mg of 3-[1-(2,4-dimethoxy-benzyl)-2-oxo-2,5-dihydro-1H-pyrrol-3-yl]-propionic acid (160 (yield: 80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07723376B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-9025fe77a5c04de3aefe83ac031c82d5 |
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| Source note | uspto-grants-2010_05 |
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