2-Methyl-1,3-dioxolane → HCID 59771748, compound

HRID 2275694Notes

Reaction equation

HRID 2275694 reaction equation
[CH3:1][CH:2]1[O:6][CH2:5][CH2:4][O:3]1.[N:7]([Si](C)(C)C)=[N+:8]=[N-:9]>Cl[Sn](Cl)(Cl)Cl>[N:7]([CH:2]([O:3][CH2:4][CH2:5][OH:6])[CH3:1])=[N+:8]=[N-:9]

Participants

4

Procedure

To a mixture of 2-methyl dioxolane (0.897 ml, 10 mmol) and azidotrimethylsilane (1.6 ml, 12 mmol) was added SnCl4 (40 μl) at −78° C. After addition, the cooling bath was removed and the reaction was warmed up to room temperature. After 1 hr, the reaction was worked, up by partitioning between DCM (50 ml) and saturated aqueous NaHCO3 (50 ml). The aqueous layer was further extracted with DCM (20 ml). All the DCM extracts were combined, dried over MgSO4 and evaporated under reduced pressure. The residue was dissolved in 10% aqueous methanol. After 2 hr at room temperature, all the solvents were removed under reduced pressure. The title compound was obtained as a colourless oil (224 mg, 17.1%).

Workup

  1. additionAfter addition
  2. customthe cooling bath was removed
  3. customup by partitioning between DCM (50 ml) and saturated aqueous NaHCO3 (50 ml)
  4. extractionThe aqueous layer was further extracted with DCM (20 ml)
  5. dry with materialdried over MgSO4
  6. customevaporated under reduced pressure
  7. dissolutionThe residue was dissolved in 10% aqueous methanol
  8. waitAfter 2 hr at room temperature
  9. customall the solvents were removed under reduced pressure

Sources & evidence

ORD record
ord-6728cc1d00ba42d5aaf92e5232a5e345
Source dataset
uspto-grants-2015_09
Patent number
US09127314B2

Reaction notes

Loading…