Diisopropylamine → N,N-Diisopropyl-1,3,2-oxathiaphospholan-2-amine

HRID 1682430Notes

Reaction equation

HRID 1682430 reaction equation
Cl[P:2]1[S:6][CH2:5][CH2:4][O:3]1.[CH:7]([NH:10][CH:11]([CH3:13])[CH3:12])([CH3:9])[CH3:8]>CCCCC>[CH:7]([N:10]([P:2]1[S:6][CH2:5][CH2:4][O:3]1)[CH:11]([CH3:13])[CH3:12])([CH3:9])[CH3:8]

Participants

4

Procedure

Compound 1 (0.2 mol) is dissolved in n-pentane (300 mL) and diisopropylamine (0.4 mol) is added dropwise. The reaction mixture is stirred at room temperature for 30 minutes, after which diisopropylamine hydrochloride is filtered off, solvent is evaporated under reduced pressure and crude product is purified by vacuum distillation. Product 2 is obtained as the fraction boiling at 70° C./0.1 mm Hg and is characterized by 31P NMR and mass spectroscopy.

Workup

  1. filtrationafter which diisopropylamine hydrochloride is filtered off
  2. customsolvent is evaporated under reduced pressure and crude product
  3. distillationis purified by vacuum distillation

Sources & evidence

ORD record
ord-237ec903103b4018bf6ebe73376116fb
Source dataset
uspto-grants-1997_06
Patent number
US05635488

Reaction notes

Loading…