3,4-dihydro-2H-pyran → HCID 67779059, compound

HRID 128499Notes

Reaction equation

HRID 128499 reaction equation
[OH:1][CH:2]([CH2:9][NH:10][C:11](=[O:14])[CH2:12][Cl:13])[CH2:3][NH:4][C:5](=[O:8])[CH2:6][Cl:7].[O:15]1[CH:20]=[CH:19][CH2:18][CH2:17][CH2:16]1.C1(C)C=CC(S([O-])(=O)=O)=CC=1.[NH+]1C=CC=CC=1>C(Cl)Cl>[O:15]1[CH2:20][CH2:19][CH2:18][CH2:17][CH:16]1[O:1][CH:2]([CH2:9][NH:10][C:11](=[O:14])[CH2:12][Cl:13])[CH2:3][NH:4][C:5](=[O:8])[CH2:6][Cl:7]

Participants

5

Conditions

Temperature
5 °C

Procedure

To a suspension of 2-hydroxy-N,N'-1,3-propanediyl-bis(2-chloroacetamide) (12.16 g; 0.050 mol) and 3,4-dihydro-2H-pyran (6.31 g; 0.075 mol) in 350 ml of CH2Cl2, 1.25 g of pyridinium p-toluenesulfonate (PPTS) (0.005 mol ) are added in portions under stirring at a temperature of 5° C. After 30 minutes, temperature raises up to 20°-25° C. and the stirring is continued during 72 h; the solution is washed with 20% aqueous NaCl (2×100 ml), dried over Na2SO4 and concentrated to dryness under vacuum. The residue solidifies in n-hexane, and then after filtration, is crystallized from EtOH (115 ml) to obtain 14.1 g of 2-[(tetrahydro-2H-pyran-2-yl)oxy]-N,N'-1,3-propanediyl-bis(2-chloroacetamide).

Workup

  1. additionare added in portions
  2. temperaturetemperature raises up to 20°-25° C.
  3. waitthe stirring is continued during 72 h
  4. washthe solution is washed with 20% aqueous NaCl (2×100 ml)
  5. dry with materialdried over Na2SO4
  6. concentrationconcentrated to dryness under vacuum
  7. filtrationafter filtration
  8. customis crystallized from EtOH (115 ml)

Sources & evidence

ORD record
ord-f506b6d27076485b843917d830c28dfd
Source dataset
uspto-grants-1995_11
Patent number
US05464607

Reaction notes

Loading…