Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844084Generated: November 1, 2026

Ethyl bromoacetate → HCID 86701850, compound

https://huagongshe.com/reaction/1844084

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
Reactant1-Indanone, 4-bromo-HCID 98713—
SolventLithium HexamethyldisilazideHCID 2733832—
ProductHCID 86701850HCID 8670185091.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-bromoindanone (15.8 g, 75 mmol) at −78° C. was added LiHMDS (1 M in THF, 90 mL). The slight brown solution was allowed to warm up to 0° C., and was cooled again to −75° and ethyl 2-bromoacetate (9.1 mL, 82 mmol) was added dropwise. The mixture was allowed to warm up over night (−75° C. to −20° C. over 12 h). The mixture was quenched with sat. ammonium chloride and was extracted with ethyl acetate. Flash chromatography give 19.5 g of the title compound in a mixture with the starting indanone ethyl 2-[4-bromo-2-(2-ethoxy-2-oxo-ethyl)-1-oxo-indan-2-yl]acetate H9 and which was used without further purification for the next step (purity, 60% of the desired product).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946280B2
Source datasetuspto-grants-2015_02
ORD IDord-4adf2a29ad514c4aa69bc42c9f1ba7fa
Source noteuspto-grants-2015_02