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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539632Generated: October 29, 2026

Sodium Iodide → 2-Bromo-4-chloro-5-[2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]ethoxy]benzenamine

https://huagongshe.com/reaction/539632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantCesium carbonateHCID 10796—
Reactant(2-Bromoethoxy)-tert-butyldimethylsilaneHCID 3608067—
Reactant5-Amino-4-bromo-2-chlorophenolHCID 59377881—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product2-Bromo-4-chloro-5-[2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]ethoxy]benzenamineHCID 5937786687.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 5-amino-4-bromo-2-chloro-phenol (0.338 g, 1.52 mmol) in NMP (5 ml) was added cesium carbonate (0.644 g, 1.97 mmol), sodium iodide (0.228 g, 1.52 mmol) and 2-bromoethoxy tertbutyldimethylsilane (0.424 g, 1.97 mmol). The mixture was heated to 100° C. for two hours, then cooled to room temperature. Water was added and the mixture was extracted with EtOAc. The combined organic extracts were washed with water and brine, dried over MgSO4, filtered and concentrated to dryness under reduced pressure. Purification of the residue by flash chromatography (hex:EtOAc/8:2) gave 2-bromo-5-[2-(tert-butyl-dimethyl-silanyloxy)-ethoxy]-4-chloro-phenylamine (0.505 g, 78%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871760B2
Source datasetuspto-grants-2014_10
ORD IDord-ffa1166fa7124cdcbd91c9e0312e0e9d
Source noteuspto-grants-2014_10