Hydrochloric Acid → HCID 10729320, compound

Temperature

-50 °C

To an ethyl ether solution (12 ml) containing 3-[(ethoxycarbonyl)oxy]-1,2-nonadiene (424 mg, 2.0 mmol) and tetraisopropoxytitanium (0.89 ml, 3.0 mmol) was added at −78° C. an ethyl ether solution containing isopropylmagnesium bromide (6.0 mmol). The reaction liquid was heated to −50° C. over 30 minutes and stirred for 1 hour. The reaction liquid was given dropwise a tetrahydrofuran solution (4 ml) containing iodine (761 mg, 3.0 mmol). After heating to 0° C. over 1.5 hours, the reaction liquid was given 3N hydrochloric acid (4 ml) and separated into layers. The organic layer was washed with a saturated aqueous solution of sodium thiosulfate and a saturated aqueous solution of sodium hydrogen carbonate, dried with anhydrous magnesium sulfate, and freed of solvent by vacuum distillation. The residues were purified by silica gel chromatography. There was obtained 385 mg of (E)-2-iodo-1,3-nonadiene as an iodinated compound (yield: 77%).

1. customThe reaction liquid
2. customThe reaction liquid
3. temperatureAfter heating to 0° C. over 1.5 hours
4. customthe reaction liquid
5. customseparated into layers
6. washThe organic layer was washed with a saturated aqueous solution of sodium thiosulfate
7. dry with materiala saturated aqueous solution of sodium hydrogen carbonate, dried with anhydrous magnesium sulfate
8. distillationfreed of solvent by vacuum distillation
9. customThe residues were purified by silica gel chromatography

ORD record

ord-dafd19e58cb84c2b972020dc288ff3cc

Source dataset

uspto-grants-2005_03

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06867161B1