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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81549Generated: October 25, 2026

Benzene, 1-bromo-3-iodo- → 2-(3-Bromo-phenyl)-2-tert-butoxycarbonylamino-3,3,3-trifluoro-propionic acid ethyl ester

https://huagongshe.com/reaction/81549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzene, 1-bromo-3-iodo-HCID 11561—
ReactantEthyl 2-((tert-butoxycarbonyl)imino)-3,3,3-trifluoropropanoateHCID 5706451—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Product2-(3-Bromo-phenyl)-2-tert-butoxycarbonylamino-3,3,3-trifluoro-propionic acid ethyl esterHCID 66665703—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 5.66 g (20 mmol) 1-bromo-3-iodo-benzene in 25 ml THF was stirred at −20° C. A 1.82 M solution of isopropylmagnesium chloride (12.1 ml, 22.0 mmol) in THF was added and the mixture was stirred 1 h at 0° C. The mixture was cooled to −78° C. and a solution of 5.38 g (20 mmol) 2-[(E)-tert-butoxycarbonylimino]-3,3,3-trifluoro-propionic acid ethyl ester in 50 ml of THF was added over a period of 2 h. After 20 min the mixture was quenched with 5% aqueous NH4Cl. The mixture was extracted with TBME. The organic phase was dried with Na2SO4, filtered and evaporated. Purification via chromatography on silica gel (c-hexane/0-14% EtOAc) gave the desired product as a colorless resin.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846658B2
Source datasetuspto-grants-2014_09
ORD IDord-0fe51288042c4bebbc75f7123b607156
Source noteuspto-grants-2014_09