HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → HCID 131718346, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 67851956 | HCID 67851956 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | HCID 131718346 | HCID 131718346 | — |
Reaction Steps
The acid 1 (59 mmol), N-bromosuccinimide (59 mmol), and azobis (2-methyl-propionitrile) (0.5 g, 3 mmol) is combined in 200 mL of Ac2O and stirred at 120°-130° C. for about 0.5 hours. When the color lightens, the solution is poured onto ice. The yellow solid is collected and dissolved in CHCl3. The CHCl3 solution is dried using Na2SO4, concentrated to a small volume, and chromatographed on silica gel column (benzene) to yield the brominated acid (5-bromomethyl-1,4-naphthoquinonyl thio)-proprionic acid, designated as compound 1b.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05292873 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-794f053e9b5f471ea1e66446df3829ed |
| Source note | uspto-grants-1994_03 |