Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29060Generated: October 25, 2026

Dimethylformamide → But-3-enyl-((S)-1-phenyl-ethyl)-amine

https://huagongshe.com/reaction/29060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantHomoallyl bromideHCID 21241—
Reactant2-NaphthylalanineHCID 185915—
SolventDiethyl EtherHCID 3283—
ProductBut-3-enyl-((S)-1-phenyl-ethyl)-amineHCID 1055917376.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of S-(−)-1-phenyl ethylamine (15.75 g, 130 mmol) in 150 mL of DMF at 0° C. is added K2CO3 (53.9 g, 390 mmol) in small portions. After stirring at 0° C. for 10 min, 4-bromobutene (13.5 g, 100 mmol) is added dropwise and followed by Nal (58.5 g, 390 mmol) in small portions. The reaction mixture, a white suspension, is heated to 95° C. and stirred overnight/16 hrs. The solution is cooled to RT and diluted with 200 mL of ether, and washed with 3×100 ml of water. The organic layer is dried over Na2SO4 and concentrated. The crude product is purified by distillation (65˜70° C. under high vacuum) to yield a colorless liquid(13.5 g, 76.7%). (NMR and MS data confirmed, U-4117-28-23).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07419975B2
Source datasetuspto-grants-2008_09
ORD IDord-e18d2c92ed544433ac683fe4fc95cb76
Source noteuspto-grants-2008_09