Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46166Generated: October 28, 2026

tert-Butyl bromoacetate → HCID 58415621, compound

https://huagongshe.com/reaction/46166

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl bromoacetateHCID 79177—
Reactant5-(4-Bromophenyl)-5H-imidazo[2,1-A]isoindoleHCID 58415514—
SolventTetrahydrofuranHCID 8028—
SolventCyclohexaneHCID 8078—
ProductHCID 58415621HCID 58415621—

Reaction Steps

To a solution of 5-(4-bromophenyl)-5H-imidazo[2,1-a]isoindole (3.17 g) in THF (60 mL) at −78° C. was added LAD solution (10.19 mL, 1.5 M in cyclohexane) drop wise. After stirring for 5 minutes tert-butyl bromoacetate was added, cooling bath was removed and the reaction mixture was stirred at room temperature. After 1.5 h the reaction was quenched with aqueous saturated NH4Cl and layers were separated. Aqueous layer was extracted with EtOAc (2×). Combined organic layers were dried over Na2SO4 and concentrated. Flash chromatography using a linear gradient of 1-50% EtOAc in hexanes afforded title compound as a white solid. Mass. found (M+H)+, 427.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541595B2
Source datasetuspto-grants-2013_09
ORD IDord-c2442bf4b791480ea2b180a4e10d079c
Source noteuspto-grants-2013_09