HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium Hydroxide → 3-Bromo-2-(((tert-butoxycarbonyl)amino)methyl)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Tert-butyl 4-bromo-1-oxoisoindoline-2-carboxylate | HCID 86593478 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Bromo-2-(((tert-butoxycarbonyl)amino)methyl)benzoic acid | HCID 22136828 | 86.3% |
Reaction Steps
To a stirred solution of 4-bromo-1-oxo-1,3-dihydro-isoindole-2-carboxylic acid tert butyl ester (0.206 g, 0.66 mmol) in tetrahydrofuran (10 ml) was added dropwise a solution of aq. lithium hydroxide (1M, 2 ml, 1.98 mmol) and the mixture stirred at room temperature under nitrogen for 18 hours. The mixture was diluted with diethyl ether (30 ml) and washed with 1M HCl (10 ml). The aqueous layer was extracted with diethyl ether (2×20 ml) and the combined organics dried over magnesium sulfate, filtered and the solvent removed by evaporation under reduced pressure to give the title compound (0.188 g, 86%) as a white waxy solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07053122B2 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-b3dc4b68f1324c3fb040b4a8f77f7796 |
| Source note | uspto-grants-2006_05 |