Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantWaterHCID 962—
Reactant3-Acetyl-5-bromopyridineHCID 820423—
ReactantSodium borohydrideHCID 4311764—
Product1-(5-Bromopyridin-3-yl)ethan-1-amineHCID 71099674—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260408B2
Source datasetuspto-grants-2016_02
ORD IDord-678fb690ab6a4e6eabe05ec5e524158d
Source noteuspto-grants-2016_02