HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774851Generated: November 4, 2026
Ammonia → 1-(5-Bromopyridin-3-yl)ethan-1-amine
https://huagongshe.com/reaction/1774851
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 3-Acetyl-5-bromopyridine | HCID 820423 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Product | 1-(5-Bromopyridin-3-yl)ethan-1-amine | HCID 71099674 | — |
Reaction Steps
To a solution of 1-(5-bromo-pyridin-3-yl)-ethanone (400 mg, 2 mmol) in methanolic ammonia (10 mL) was added Ti(O-iPr)4 (1.14 g, 4 mmol). The resulting reaction mixture was heated to reflux and stirred over night. After cooling at 0° C., NaBH4 was added into the mixture and it was allowed to warm up to room temperature and stirred for 3 hours. Water was added and the reaction mixture was extracted with EtOAc. The organic layer was washed with water and brine, dried over anhydrous Na2SO4, filtered and concentrated in vacuo. It was directly used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09260408B2 |
|---|
| Source dataset | uspto-grants-2016_02 |
|---|
| ORD ID | ord-678fb690ab6a4e6eabe05ec5e524158d |
|---|
| Source note | uspto-grants-2016_02 |
|---|