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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1511366Generated: October 26, 2026

Ammonia → 1-(4-Bromo-2-chlorophenyl)ethanamine

https://huagongshe.com/reaction/1511366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant1-(4-Bromo-2-chlorophenyl)ethan-1-oneHCID 15560950—
CatalystTitanium isopropoxideHCID 11026—
SolventMethanolHCID 887—
Product1-(4-Bromo-2-chlorophenyl)ethanamineHCID 59843034—

Reaction Conditions

Temperature45 °C

Reaction Steps

A solution of 1-(4-bromo-2-chlorophenyl)ethanone (2.430 g, 10 mmol), ammonia, 2.0 m solution in methanol (26 ml, 52 mmol) and titanium (iv) isopropoxide (6 ml, 21 mmol) was stirred for 16 h in a sealed vessel. Reaction then added to a freshly made suspension of sodium borohydride powder, 98% (4 g, 104 mmol) in MeOH (20 mL). Exothermic reaction started at 9:45 am, then continued to stir with a 45° C. external heating bath for 45 min. Water (10 mL) then added to reaction and stirred for an additional 10 min. Resulting white solid removed via filtration through Celite, and filtrated reduced in volume under reduced pressure. This suspension then partioned between 9:1 CHCl3/IPA (30 mL) and 1M NaOH (10 mL). Aqueous further extracted with 9:1 CHCl3/IPA (2×10 mL). Combined organics dried over MgSO4, concentrated, then purified on silica (80 g) eluting with 0>5% 2M NH3 in MeOH/DCM. MS (ESI pos. ion) m/z: 234/236 (MH+). Calc'd exact mass for C8H9BrClN: 233/235. 1-(4-bromo-2-chlorophenyl)ethanamine isolated as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08212041B2
Source datasetuspto-grants-2012_07
ORD IDord-48f3d5181cce49e9a1e3f2668a1de358
Source noteuspto-grants-2012_07