HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → (3R)-6-carboxy-5-oxo-1-thia-4-azacyclotridecane-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 54302673 | HCID 54302673 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (3R)-6-carboxy-5-oxo-1-thia-4-azacyclotridecane-3-carboxylic acid | HCID 54274042 | — |
Reaction Steps
Methyl (3R)-6-methoxycarbonyl-5oxo-1-thia-4-azacyclotridecane-3-carboxylate (2.39 g, 7.21 mmol) is suspended in methanol (75 ml) and 1N sodium hydroxide (22.0 ml, 22.0 mmol) is added. The mixture is stirred for 4 hours at room temperature. The solvent is evaporated and the residue is dissolved in water (150 ml). The aqueous solution is adjusted to pH 1 by addition of 1N hydrochloric acid and extracted with ethyl acetate (3×100 ml). The combined extracts are washed with brine (1×100 ml), dried (MgSO4) and the solvent is evaporated to give (3R)-6-carboxy-5-oxo-1-thia-4-azacyclotridecane-3-carboxylic acid, m.p. 167°-170° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05244889 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-d95927d178064a35970f180e99ed80b8 |
| Source note | uspto-grants-1993_09 |