Sodium Iodide → methyl 4-(4-bromo-2-nitrophenyl)tetrahydro-2H-pyran-4-carboxylate

Sodium hydride (0.32 g, 8.03 mmol, 60% dispersion in oil) was added in portions at rt to a stirred solution of methyl 2-(4-bromo-2-nitrophenyl)acetate (1 g, 3.65 mmol) in DMSO (15 mL). After the mixture was stirred at rt for 30 min, sodium iodide (0.055 g, 0.365 mmol) and bis(2-bromoethyl)ether (1.27 g, 5.47 mmol) were added. The resultant mixture was stirred at 40° C. After 19 h, the mixture was poured into brine with ice (50 mL) and extracted with EtOAc (3×50 mL). The combined extracts were washed with brine (3×80 mL), dried over Na2SO4, filtered, and evaporated in vacuo. The residue was purified by column chromatography (0 to 50% gradient of EtOAc in n-hexane) to give methyl 4-(4-bromo-2-nitrophenyl)tetrahydro-2H-pyran-4-carboxylate as an orange syrup. Mass Spectrum (ESI) m/e=344 [(M+1) (79Br)] and 346 [(M+1) (81Br)].

1. waitAfter 19 h
2. extractionextracted with EtOAc (3×50 mL)
3. washThe combined extracts were washed with brine (3×80 mL)
4. dry with materialdried over Na2SO4
5. filtrationfiltered
6. customevaporated in vacuo
7. customThe residue was purified by column chromatography (0 to 50% gradient of EtOAc in n-hexane)

ORD-Eintrag

ord-c977364b063a4c0ab80bd643066fe1d8

Quelldatensatz

uspto-grants-2014_07

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08765940B2