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 0.5 N 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 | US04900674 |
| Source dataset | uspto-grants-1990_02 |
| ORD ID | ord-fa7d20cdee8f4c599c704dd8fe1ce134 |
| Source note | uspto-grants-1990_02 |