HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 2-(4-Boc-piperazinyl)-2-(2-methylphenyl)acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 69430358 | HCID 69430358 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(4-Boc-piperazinyl)-2-(2-methylphenyl)acetic acid | HCID 2762227 | 86.9% |
Reaction Steps
To 4-(Ethoxycarbonyl-o-tolyl-methyl)-piperazine-1-carboxylic acid tert-butyl ester (152) (0.83 g, 2.27 mmol) in EtOH (10 mL) was added NaOH (0.46 g, 11.38 mmol) and the mixture stirred at room temperature for 18 h. The reaction mixture was then concentrated to dryness. The resulting residue was taken up in H2O (100 mL) and acidified (pH=4–6) with 25% KHSO4, and the desired acid was extracted into EtOAc (100 mL). The organic phase was washed with H2O (100 mL) and brine (100 mL) and concentrated to dryness yielding 0.66 g (86%) pure product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07169777B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-442063a2bfb64fed8f8ac0623953cb47 |
| Source note | uspto-grants-2007_01 |