Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Butyl-N-nitrosobutyramide | HCID 149617 | — |
| Reactant | Jeffamine | HCID 15131492 | — |
| Reactant | Chloroform methanol acetic acid water | HCID 21923999 | — |
| Product | Jeffamine | HCID 15131492 | — |
| Product | nBBA Jeffamine | HCID 131716719 | — |
Reaction Steps
Polyoxypropylenepolyamines and polyoxyethylenepolyamines (referred to as "Jeffamines", a trademark of Jefferson Chemical Co., Inc.) were photolabeled by coupling the N-oxysuccinimide ("NOS") esters of ANP-EACA, BBA and nBBA to the polymers. These NOS-derivatives were added in 0.5X amounts to 1X Jeffamine in very dry (high purity) solvents (ANP-EAC-NOS in dry tetrahydrofuran, BBA-NOS in dry dioxane or dimethylformamide and nitro BBA-NOS in dry dioxane or dimethylformamide). After 16 hours of reaction at room temperature in the dark, the products were isolated by TLC in 85/15/1/1/ chloroform/methanol/H2O/acetic acid. Monosubstituted Jeffamine derivatives were extracted with the TLC solvent and azeotrophed with water to remove the residual acetic acid. The water soluble products ANP-EAC-Jeffamine, BBA-Jeffamine, and nBBA-Jeffamine were isolated in 15%, 10% and 12% yields, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04973493 |
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| Source dataset | uspto-grants-1990_11 |
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| ORD ID | ord-673b1742801c4b41a591ca677c9f3b75 |
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| Source note | uspto-grants-1990_11 |
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