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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2388028Generated: October 31, 2026

1,2-Dichloroethane → 4-[(5-Bromopyridin-3-yl)acetyl]morpholine

https://huagongshe.com/reaction/2388028

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantMorpholineHCID 8083—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant2-(5-Bromopyridin-3-yl)acetic acidHCID 2802539—
SolventDichloromethaneHCID 6344—
Solvent3',3',6-Trimethyl-5-nitro-1',2',3',6'-tetrahydro-3,4'-bipyridineHCID 67336722—
Product4-[(5-Bromopyridin-3-yl)acetyl]morpholineHCID 1898599495%

Reaction Steps

To a solution of (5-bromopyridin-3-yl)acetic acid (1.00 g, 4.63 mmol) and morpholine (0.50 mL, 5.73 mmol) in DCM (50 mL) was added EDC (1.78 g, 9.30 mmol) and 1-hydroxybenzotriazole (1.25 g, 9.26 mmol). The reaction mixture was allowed to stir at rt for 50 min and then diluted with DCM (50 mL) and 1N HCl (100 mL). The organic solution was separated and discarded. The aqueous solution was neutralized with sat. aq. NaHCO3 (100 mL) and was extracted with DCM (3×50 mL). The organic solutions were combined, dried over MgSO4, filtered and concentrated to give 4-[(5-bromopyridin-3-yl)acetyl]morpholine (1.26 g, 4.40 mmol, 95%) as a light brown solid. LCMS (FA): Rt=1.11 min, m/z=287.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268992B2
Source datasetuspto-grants-2012_09
ORD IDord-cbb9d12fcdec44d48fe4f50bfa52b47a
Source noteuspto-grants-2012_09