Water → (R)-4-azido-chroman-7-carbonitrile

Temperature

0 °C

Azeotropically dried (S)-4-hydroxy-chroman-7-carbonitrile (2.0 g, 11 mmol) was dissolved in dry THF (55 ml). DPPA (3.0 ml, 3.8 g, 14 mmol) was added to the solution at RT and the mixture was stirred for 5 min. The solution was cooled to 0° C. and 1,8-diazabicyclo[5,4,0]undec-7-ene (2.0 mL, 2.1 g, 14 mmol) was added. After stirring for 10 min at 0° C., the reaction was warmed to RT, at which time a white precipitate formed, and was stirred for 14 h. The resulting solution was poured into H2O (100 mL) and extracted with Et2O (300 mL, 3×). The organic phases were combined, washed with brine, dried over MgSO4, filtered and concentrated in vacuo to provide a residue which was purified by flash column chromatography (silica, 33% hexane in CH2Cl2) to provide the title compound.

1. stirringAfter stirring for 10 min at 0° C.
2. temperaturethe reaction was warmed to RT, at which time a white precipitate
3. customformed
4. stirringwas stirred for 14 h
5. extractionextracted with Et2O (300 mL, 3×)
6. washwashed with brine
7. dry with materialdried over MgSO4
8. filtrationfiltered
9. concentrationconcentrated in vacuo
10. customto provide a residue which
11. customwas purified by flash column chromatography (silica, 33% hexane in CH2Cl2)

ORD record

ord-b072df2c26cc4bbfb403273e9f298f1b

Source dataset

uspto-grants-2007_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07199244B2