Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261730Generated: November 3, 2026

N-bromobutanimide → Ethyl 3-cyclopropyl-2-oxopropanoate

https://huagongshe.com/reaction/2261730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantMethylenechloride HexaneHCID 21226440—
ReactantEthyl 2-(cyclopropylmethyl)-1,3-dithiane-2-carboxylateHCID 22285400—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductEthyl 3-cyclopropyl-2-oxopropanoateHCID 2228562961.2%

Reaction Steps

To a 0° C. suspension of NBS (439 mmol, 79 g) in a mixture of acetonitrile (400 mL) and water (100 mL) is added a solution of 2-cyclopropylmethyl-[1,3]dithiane-2-carboxylic acid ethyl ester (73.2 mmol, 18.05 g) in acetonitrile (50 mL) over 15 minutes. The reaction is warmed and is stirred at room temperature. After 45 minutes, 500 mL of 1:1 hexane/DCM is added. The layers are separated. The organic layer is washed with saturated Na2SO3 (2×225 mL) and brine (2×225 mL), dried with Na2SO4, filtered, and concentrated under reduced pressure to a residue. The residue is diluted in CCl4 and is filtered. The filtrate is concentrated to give the title compound (7 g, 61%). LC-MS: 157.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846960B2
Source datasetuspto-grants-2010_12
ORD IDord-1ae2d0e3f2fc4bcd8b36543131a01205
Source noteuspto-grants-2010_12