Back
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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Pyrenebutanoic acidHCID 76977—
ReactantN-HydroxysuccinimideHCID 80170—
Reactant1,3-DichlorohexylcarbodiimideHCID 22046199—
SolventDimethyl SulfoxideHCID 679—
ProductSuccinimidyl-1-pyrenebutanoic acidHCID 1845959570%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432632B1
Source datasetuspto-grants-2002_08
ORD IDord-240cf8c13a6e4ae7871d5a2874f03dd3
Source noteuspto-grants-2002_08