HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → mono N-hydroxysuccinimide glutarate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Glutaric anhydride | HCID 7940 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | mono N-hydroxysuccinimide glutarate | HCID 19793121 | — |
Reaction Steps
One mole of glutaric anhydride and one mole of N-hydroxysuccinimide were treated in dichloromethane with 1.2 equivalents of triethylamine. This reaction was stirred for 40 minutes, acidified by the addition of 0.5N hydrochloric acid (HCl) (aqueous), and then extracted with ethyl acetate to form mono N-hydroxysuccinimide glutarate. This glutarate was then combined with 5 moles of thionyl chloride and stirred at room temperature for three hours. The resulting reaction mixture was dried to remove volatiles, and thereby form N-hydroxysuccinimidyl glutaryl chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05248611 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-1ed7b4f414b94a45a886575dff6a9247 |
| Source note | uspto-grants-1993_09 |