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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118586Generated: October 30, 2026

tert-Butyl bromoacetate → HCID 20028930, compound

https://huagongshe.com/reaction/2118586

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl bromoacetateHCID 79177—
Reactant2-chloro-1H-imidazoleHCID 2773328—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventDichloromethaneHCID 6344—
ProductHCID 20028930HCID 20028930—

Reaction Steps

The starting material was prepared by reaction of 2-chloroimidazole with t-butyl bromoacetate in CH2Cl2 /aqueous sodium hydroxide in presence of tetra-n-butyl ammonium hydrogen sulphate to give 1-t-butoxycarbonylmethyl-2-chloroimidazole. Reaction of this compound with trimethyloxonium tetrafluoroborate in CH2Cl2 gave 1-t-butoxycarbonylmethyl-2-chloro-3-methylimidazolium tetrafluoroborate; n.m.r. in d6DMSO: 1.5 (s, 9H); 3.9 (s, 3H); 5.17 (s, 2H); 7.81 (d, 1H): 7.85 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04678781
Source datasetuspto-grants-1987_07
ORD IDord-cc4afa283278458cb385d75f511a825c
Source noteuspto-grants-1987_07