Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 6-(4-Nitro-1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)hexanoic acid | HCID 303582 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 20291877 | HCID 20291877 | 94% |
Reaction Steps
2.58 ml (0.018 mol) of triethylamine, followed by 1.3 g (0.0198 mol) of sodium azide, are added to a mixture of 5.7 g (0.018 mol) of 6-(3-nitrophthalimidyl)-caproic acid in 35 ml of dimethylsulphoxide. The reaction mixture is heated for 6 hours at 50° C. and is then concentrated in vacuo, diluted with 100 ml of water and acidified with 4 ml of concentrated hydrochloric acid. The resulting suspension of the reaction product is stirred for 18 hours and filtered with suction, and the filter residue is washed with 20 ml of water and dried for 24 hours at 60° C./0.100. mm Hg, over phosphorus pentoxide. 5.1 g (94% of theory) of 6-(3-azidophthalimidyl)-caproic acid are obtained; melting point 87°-90° C. (with decomposition). IR spectrum (CH2Cl2): 1780 and 1725 cm-1 (CO--N--CO); 2130 cm-1 (N3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04250096 |
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| Source dataset | uspto-grants-1981_02 |
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| ORD ID | ord-b3148f537cf5496c8ccd06d8e655dec5 |
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| Source note | uspto-grants-1981_02 |
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