HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2302133Generated: October 25, 2026
1-Pyrenebutanoic acid → Succinimidyl-1-pyrenebutanoic acid
https://huagongshe.com/reaction/2302133
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Pyrenebutanoic acid | HCID 76977 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | 1,3-Dichlorohexylcarbodiimide | HCID 22046199 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | Succinimidyl-1-pyrenebutanoic acid | HCID 18459595 | 70% |
Reaction Steps
SPB was prepared according to the synthesis scheme shown in FIG. 2. In 20 ml of dimethylsulfoxide (DMF), 2.25 g of 1-pyrenebutanoic acid (7.8 mmol: obtained from Molecular Probes, Inc.) and 1.2 g of N-hydroxy succinimide (10.4 mmol: obtained from Wako Pure Chemical Industries, Ltd.) were dissolved. After the mixed solution was cooled to 0° C., 2.69 g of 1,3-dichlorohexylcarbodiimide (13.1 mmol: DCC) was added thereto. Then, the mixture was reacted at 0° C. for 24 hours while stirring. After the reacted solution was filtered with a 0.45 μm filter, the filtrate was collected and dried using an evaporator. Then, the filtrate was recrystallized from 95% ethanol, thereby obtaining 1.88 g of succinimidyl-1-pyrenebutanoic acid (yield: 70%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06432632B1 |
|---|
| Source dataset | uspto-grants-2002_08 |
|---|
| ORD ID | ord-240cf8c13a6e4ae7871d5a2874f03dd3 |
|---|
| Source note | uspto-grants-2002_08 |
|---|