3,4-dihydro-2H-pyran → HCID 67779059, compound
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
- additionare added in portions
- temperaturetemperature raises up to 20°-25° C.
- waitthe stirring is continued during 72 h
- washthe solution is washed with 20% aqueous NaCl (2×100 ml)
- dry with materialdried over Na2SO4
- concentrationconcentrated to dryness under vacuum
- filtrationafter filtration
- customis crystallized from EtOH (115 ml)
Sources & evidence
- ORD record
- ord-f506b6d27076485b843917d830c28dfd
- Source dataset
- uspto-grants-1995_11
- Patent number
- US05464607
Reaction notes
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