HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoacetic Acid → Iodoacetic acid N-hydroxysuccinimide ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoacetic Acid | HCID 5240 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Iodoacetic acid N-hydroxysuccinimide ester | HCID 3299230 | 71% |
Reaction Steps
N-Hydroxysuccinimide (1 g, 8.7 mmole), iodoacetic acid (8.7 mmole, 1.6 g), and DCC (8.7 mmole, 1.7 g) were added to 250 mL of EtOAc and the mixture was stirred at room temperature for 5 hours. The mixture was filtered and the filtrate concentrated to dryness in vacuo. The residue was crystallized from ethanol to yield 1.74 g (71%) of white crystals, mp 148-150° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06160128 |
| Source dataset | uspto-grants-2000_12 |
| ORD ID | ord-5627ecce1c4349c0b967f59e94f1ad71 |
| Source note | uspto-grants-2000_12 |