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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | (2-Bromoethoxy)-tert-butyldimethylsilane | HCID 3608067 | — |
| Reactant | 5-Amino-4-bromo-2-chlorophenol | HCID 59377881 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 2-Bromo-4-chloro-5-[2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]ethoxy]benzenamine | HCID 59377866 | 87.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08871760B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-ffa1166fa7124cdcbd91c9e0312e0e9d |
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| Source note | uspto-grants-2014_10 |
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