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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114347Generated: October 30, 2026

Acetic Acid → [1-(3-Bromophenyl)-2-(4-morpholinyl)ethyl]methylamine

https://huagongshe.com/reaction/2114347

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethylamineHCID 6329—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant1-(3-Bromophenyl)-2-(4-morpholinyl)ethanoneHCID 20823746—
SolventTetrahydrofuranHCID 8028—
Product[1-(3-Bromophenyl)-2-(4-morpholinyl)ethyl]methylamineHCID 57501274100.3%

Reaction Steps

To a solution of 1-(3-bromophenyl)-2-(4-morpholinyl)ethanone (7.8 g, 27.0 mmol) in THF (50 mL) was added methylamine (100 mL, 200 mmol, 2M solution in THF). After stirring for 15 min at room temperature, sodium cyanoborohydride (3.40 g, 54 mmol) was added followed by acetic acid (2 mL). The resultant mixture was stirred at RT for 5 days. The mixture was concentrated under reduced pressure. The residue was dissolved in ethyl acetate (200 mL) and washed with 5% NaHCO3 (200 mL) and brine (200 mL). The organic layer was dried (MgSO4) and concentrated to give [1-(3-bromophenyl)-2-(4-morpholinyl)ethyl]methylamine as yellow oil (8.10 g, 100%) which solidified after standing at room temperature. MS (ESI): 299.6 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432258B2
Source datasetuspto-grants-2008_10
ORD IDord-af173e9b66af485e88b2a2aae1d99e84
Source noteuspto-grants-2008_10