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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712739Generated: October 29, 2026

Acetyl chloride → HCID 117667398, compound

https://huagongshe.com/reaction/712739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 117667434HCID 117667434—
SolventDichloromethaneHCID 6344—
ProductHCID 117667398HCID 117667398—

Reaction Steps

To a vial is added (1R)-1-(5-bromo(3-pyridyl))ethylamine HCl (500 mg, 2.1 mmol) in 2.5 ml of DCM, followed by the addition of N,N-diisopropylethylamine (816 mg, 2.52 mmol). Then acetyl chloride 1M in DCM solution (2.5 ml, 2.5 mmol) is added at 0° C. The reaction mixture is stirred at room temperature for 2 hours. The reaction mixture is diluted with DCM, washed with water, brine, dried over anhydrous Na2SO4, filtered and concentrated to give the crude product. Purification by the flash column chromatography affords 273 mg of N-[(R)-1-(5-bromo-pyridin-3-yl)-ethyl]-acetamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181272B2
Source datasetuspto-grants-2015_11
ORD IDord-57a49f10f98742139c21244b7c429771
Source noteuspto-grants-2015_11