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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930772Generated: October 31, 2026

1,2-Dimethoxyethane → Di-tert-butyl{3-[3-(bromomethyl)isoxazol-5-yl]pyridin-2-yl}imidodicarbonate

https://huagongshe.com/reaction/1930772

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantTriethylamineHCID 8471—
ReactantPhosphorus tribromideHCID 24614—
ReactantDi-tert-butyl{3-[3-(hydroxymethyl)isoxazol-5-yl]pyridin-2-yl}imidodicarbonateHCID 57867426—
SolventWaterHCID 962—
ProductDi-tert-butyl{3-[3-(bromomethyl)isoxazol-5-yl]pyridin-2-yl}imidodicarbonateHCID 5786741815.4%

Reaction Steps

To a mixture of di-tert-butyl{3-[3-(hydroxymethyl)isoxazol-5-yl]pyridin-2-yl}imidodicarbonate (0.78 g, 2 mmol), triethylamine (1.95 mL, 14 mmol) and 1,2-dimethoxyethane (10 mL) was added phosphorus tribromide (0.37 mL, 4 mmol) dropwise at 0° C., which was stirred at room temperature for two hours, and then stirred at 50° C. for 30 minutes. The reaction mixture was cooled to 0° C., then water was added thereto and extracted with ethyl acetate, and the organic layer was washed with saturated sodium chloride water. After drying over anhydrous magnesium sulfate and filtering, the solvent was evaporated under a reduced pressure, the residue was purified by silica gel column chromatography to obtain the title compound (0.14 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188119B2
Source datasetuspto-grants-2012_05
ORD IDord-05df349dbb894799866e23703ddffd95
Source noteuspto-grants-2012_05