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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253481Generated: November 2, 2026

Water → N-(4-Bromobutyl)-2,2,2-trifluoro-N-isopropylacetamide

https://huagongshe.com/reaction/253481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,4-DibromobutaneHCID 8056—
ReactantSodium hydrideHCID 24758—
Reactant2,2,2-Trifluoro-N-isopropylacetamideHCID 2305253—
SolventDimethylformamideHCID 6228—
ProductN-(4-Bromobutyl)-2,2,2-trifluoro-N-isopropylacetamideHCID 8605328524%

Reaction Conditions

Temperature0 °C

Reaction Steps

21 g (520 mmol) of 60% sodium hydride are suspended in 700 ml of anhydrous DMF under an inert atmosphere, and the mixture is cooled to 0° C. 40.5 g (260 mmol) of 2,2,2-trifluoro-N-isopropylacetamide are slowly added portionwise. After 15 minutes, 62 ml (520 mmol) of 1,4-dibromobutane are added. The reaction medium is then heated at 60° C. for 3 hours, and then cooled to room temperature, poured into 1 L of water and extracted with ethyl acetate. The organic phase is washed with water and dried, and the residue obtained is purified by distillation. A colorless oil is obtained (m=0.18 g, yield=24%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872026B2
Source datasetuspto-grants-2011_01
ORD IDord-3a38f05933324537af6e6a51d9eeba64
Source noteuspto-grants-2011_01