Iodine → 3-iodo-4,4-dimethoxytetrahydro-2H-pyran

Temperature

0 °C

To a mixture of tetrahydro-4H-pyran-4-one (18.52 mL, 200 mmol) and trimethyl orthoformate (100 mL, 914 mmol) at 0° C. was added Iodine (49.2 mL, 200 mmol) slowly over 10 min. When the addition was complete, the reaction mixture was allowed to stir at 0° C. for 30 min. and was then allowed to come to RT and stir until TLC indicated all starting material had been consumed (approx. 1 h). The reaction was then cooled to 0° C. and quenched by the slow addition of sat. aqu. sodium thiosulfate (300 mL). The resulting mixture was extracted with EtOAc (3×75 mL). The combined organic layers were washed with brine (100 mL), dried over MgSO4, filtered and concentrated in vacuo. Purification by flash chromatography (Silica, EtOAc/Hexanes) gave 3-iodo-4,4-dimethoxytetrahydro-2H-pyran (43.95 g, 162 mmol, 81% yield) as a yellow oil. 1H NMR (500 MHz, CDCl3) δ ppm 4.25 (1 H, q, J=2.44 Hz), 3.93-4.01 (1 H, m), 3.84-3.93 (2 H, m), 3.57 (1 H, td, J=11.75, 2.44 Hz), 3.19-3.30 (6 H, m), 2.34 (1 H, ddd, J=14.34, 12.21, 4.88 Hz), 1.80 (1 H, dq, J=14.34, 2.44 Hz).

1. additionWhen the addition
2. customto come to RT
3. stirringstir until TLC
4. customhad been consumed (approx. 1 h)
5. temperatureThe reaction was then cooled to 0° C.
6. customquenched by the slow addition of sat. aqu
7. extractionThe resulting mixture was extracted with EtOAc (3×75 mL)
8. washThe combined organic layers were washed with brine (100 mL)
9. dry with materialdried over MgSO4
10. filtrationfiltered
11. concentrationconcentrated in vacuo
12. customPurification by flash chromatography (Silica, EtOAc/Hexanes)

ORD record

ord-08acb5fb384d4f0e9aa666327d993f06

Source dataset

uspto-grants-2014_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08710061B2