HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555405Generated: October 26, 2026
N-bromobutanimide → HCID 59857539, compound
https://huagongshe.com/reaction/555405
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-(2-Tert-butylphenoxy)pyridin-3-amine | HCID 28605427 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59857539 | HCID 59857539 | 104.3% |
Reaction Steps
A solution of N-bromosuccinimide (2.32 g, 13.0 mmol) in DMF (20 ml) was added to a cold (−20° C.) solution of 1b (2.76 g, 11.4 mmol) in DMF (25 ml). The reaction rapidly turned dark red. HPLC analysis after 5 min showed that the reaction was complete. The reaction was quenched with a freshly prepared solution of sodium thiosulfate (40 ml, 10% aqueous). A precipitate formed. The mixture was warmed to rt and was diluted with water (60 ml). The solid was filtered, washed with water and dried overnight under reduced pressure to give 123a (3.82 g, 96% yield) as brown solid. [M+H]+=321.14. 1H NMR (500 MHz, CDCl3) δ ppm 1.40 (s, 9H), 3.91 (s, 2H), 6.93 (m, 2H), 7.00 (d, J=8.07 Hz, 1H), 7.12 (t, J=7.73 Hz, 1H), 7.20 (t, J=7.73 Hz, 1H), 7.41 (d, J=8.07 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08053450B2 |
|---|
| Source dataset | uspto-grants-2011_11 |
|---|
| ORD ID | ord-43bfd150c47f45a2be06e1abddfaa04d |
|---|
| Source note | uspto-grants-2011_11 |
|---|