HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923480Generated: October 31, 2026
Water → Di-tert-butyl [(3-bromopyridin-4-yl)methyl]imidodicarbonate
https://huagongshe.com/reaction/923480
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Di-tert-butyl Iminodicarboxylate | HCID 279800 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 3-Bromo-4-(chloromethyl)pyridine | HCID 66933309 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Di-tert-butyl [(3-bromopyridin-4-yl)methyl]imidodicarbonate | HCID 118318074 | 90.3% |
Reaction Steps
To a solution of 1.73 g of di-tert-butyl imidodicarbonate in DMF 16 ml was added 894 mg of potassium tert-butoxide under ice-cooling, followed by stirring at room temperature for 1 hour. To the reaction mixture was added a solution of 1.37 g of 3-bromo-4-(chloromethyl)pyridine in 3 ml of DMF under ice-cooling, followed by stirring at room temperature for 2 hours. To the reaction mixture was added water, followed by extraction with ethyl acetate. The organic layer was washed with water and a saturated aqueous sodium chloride solution, and dried over anhydrous magnesium sulfate, and the solvent was then evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain 2.32 g of di-tert-butyl [(3-bromopyridin-4-yl)methyl]imidodicarbonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09278968B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-028586114a174a939c375347c41a4ded |
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| Source note | uspto-grants-2016_03 |
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