1-Dodecanol → HCID 86739352, compound
Reaction equation
[O:1]1[CH2:6][CH2:5][O:4][CH2:3][C:2]1=[O:7].[CH3:8][N:9]1[C:14](=[O:15])[CH2:13][O:12][C:11](=[O:16])[CH2:10]1.C(O)CCCCCCCCCCC.CCCCC(C([O-])=O)CC.CCCCC(C([O-])=O)CC.[Sn+2]>C1(C)C=CC=CC=1>[O:1]1[CH2:6][CH2:5][O:4][CH2:3][C:2]1=[O:7].[CH3:8][N:9]1[C:14](=[O:15])[CH2:13][O:12][C:11](=[O:16])[CH2:10]1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
p-Dioxanone (28.5 g, 0.279 moles), N-methyl-2,5- morpholinedione (1.5 g, 0.01162 moles), 1-dodecanol (0.082 g, 0.00044 moles), and a catalytic amount of stannous octoate (0.06 ml of a 0.33 M toluene solution, 0.0000198 moles) are heated and magnetically mixed in a flame and vacuum dried, sealed glass ampule according to the following temperature/time scheme:
Workup
- additionmagnetically mixed in
- temperaturea flame
- customvacuum dried
- customsealed glass ampule
Sources & evidence
- ORD record
- ord-6fc0e53c921340e78ed1e0e606cff725
- Source dataset
- uspto-grants-1984_04
- Patent number
- US04441496
Reaction notes
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