HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 2,2'-(Hex-5-ynylazanediyl)diacetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 87118843 | HCID 87118843 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,2'-(Hex-5-ynylazanediyl)diacetic acid | HCID 87118722 | — |
Reaction Steps
To the obtained approximately 1.4 g dimethyl 2,2′-(hex-5-ynylazanediyl)diacetate was added 20 mL THF and 20 mL of 2 M KOH. The mixture was stirred overnight and monitored by TLC. The organic layer was separated, and the aqueous layer was quenched by addition of 20 mL of 2 M HCl. The solvent (H2O) was removed by rotary evaporation, and the resulting solid was dissolved into acetonitrile (ACN). The insoluble KCl salt was filtered, and the filtrate was concentrated by rotary evaporation. The final product of free acid was obtained as a greasy, transparent oil. Yield was quantitative. ESI-MS: [M+H]+ m/z 214.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08778626B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-349d142eb7e44a1580f1c236d3f0d03c |
| Source note | uspto-grants-2014_07 |