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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387281Generated: October 30, 2026

Dimethylformamide → HCID 59593345, compound

https://huagongshe.com/reaction/2387281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantHCID 975849HCID 975849—
ReactantHCID 178418306HCID 178418306—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59593345HCID 59593345—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To (5-Bromo-pyridin-2-yl)-(4-chloro-benzyl)-amine (56, 10.00 g, 0.03360 mol) in tetrahydrofuran (400.0 mL) under an atmosphere of nitrogen at −78° C. was added n-butyllithium (17.5 mL, 2.00 M in cyclohexane). After 90 minutes, tert-butyllithium (42.00 mL, 1.70 M in hexane) was added to the reaction. After 80 minutes, N,N-dimethylformamide (6.9 mL, 0.089 mol) was added to the reaction. The reaction mixture was stirred at −78° C. for 2 hours, then allowed to warm to room temperature for 1 hour. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate mid concentrated to give the crude compound, which was crystallized from tert-butoxyl methyl ether to provide compound (57, 7.66 g, 92.2%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268858B2
Source datasetuspto-grants-2012_09
ORD IDord-165c88b8da024f14be93fbdb4600ab60
Source noteuspto-grants-2012_09