Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264412Generated: November 1, 2026

Dimethylformamide → (RS)-2-(2-buten-1-yl)-6-ethoxy-1-indanone

https://huagongshe.com/reaction/264412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantEthyl BromideHCID 6332—
ReactantPotassium CarbonateHCID 11430—
Reactant(RS)-2-(2-buten-1-yl)-6-hydroxy-1-indanoneHCID 54363126—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product(RS)-2-(2-buten-1-yl)-6-ethoxy-1-indanoneHCID 5372986498%

Reaction Steps

A solution of 5.0 g of (RS)-2-(2-buten-1-yl)-6-hydroxy-1-indanone, 4.1 ml of ethyl bromide, 6.83 g of potassium carbonate and 10 ml of N,N-dimethyl-formamide in 70 ml of acetone was heated to 35° for 35 hours. After cooling, the solution was poured into 100 ml of water and extracted twice with 100 ml of ethyl acetate each time. The combined organic phases were washed once with 70 ml of water and once with 70 ml of saturated sodium chloride solution, dried over magnesium sulfate and the solution was concentrated in a vacuum. 5.6 g (98%) of (RS)-2-(2-buten-1-yl)-6-ethoxy-1-indanone were obtained as a red-brown oil which was used directly in the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646173
Source datasetuspto-grants-1997_07
ORD IDord-b879e159d2af41e68e730dc1dc95d348
Source noteuspto-grants-1997_07