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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722562Generated: November 3, 2026

tert-Butyl bromoacetate → HCID 20028930, compound

https://huagongshe.com/reaction/1722562

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 trimlethyloxonium 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 numberUS04855420
Source datasetuspto-grants-1989_08
ORD IDord-7ab58564d57e486eab25deffd3ea64bb
Source noteuspto-grants-1989_08