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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264416Generated: October 31, 2026

Water → (RS)-2-(2-buten-1-yl)-6-isobutoxy-1-indanone

https://huagongshe.com/reaction/264416

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Bromo-2-methylpropaneHCID 6555—
ReactantPotassium CarbonateHCID 11430—
Reactant(RS)-2-(2-buten-1-yl)-6-hydroxy-1-indanoneHCID 54363126—
SolventDimethylformamideHCID 6228—
Product(RS)-2-(2-buten-1-yl)-6-isobutoxy-1-indanoneHCID 5437473193%

Reaction Steps

A solution of 4.74 g of (RS)-2-(2-buten-1-yl)-6-hydroxy-1-indanone, 5.18 ml of isobutyl bromide and 5.98 g of potassium carbonate in 40 ml of N,N-dimethylformamide was heated to 60° for 48 hours. After cooling, the solution was poured into 100 ml of water and extracted twice with 70 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. 5.2 g (93%) of (RS)-2-(2-buten-1-yl)-6-isobutoxy-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-638846c380fc4d65ae39cc7067e9c389
Source noteuspto-grants-1997_07