Dimethylamine → HCID 70607993, compound
Reaction equation
[O:1]1[C:5](=[O:6])[CH2:4][C@@H:3]2[CH2:7][C:8]3[C:13]([CH2:14][C@@H:2]12)=[CH:12][CH:11]=[CH:10][CH:9]=3.[CH3:15][NH:16][CH3:17]>C1COCC1>[CH3:15][N:16]([CH3:17])[C:5](=[O:6])[CH2:4][C@@H:3]1[CH2:7][C:8]2[C:13](=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH2:14][C@H:2]1[OH:1]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 18.8 (0.10 mol) of trans-3a, 4,9,9a-tetrahydronaphtho[2,3-b]furan-2(3H)-one, 35 ml of anhydrous dimethylamine, and 35 ml of dry THF is heated in a small Parr bomb at 100° for 3 days. The cooled reaction mixture is then taken to dryness in vacuo, and the residue triturated with ether to give 22.5 g (97%) of crystalline solid after drying in vacuo.
Workup
- temperatureis heated in a small Parr bomb at 100° for 3 days
- customThe cooled reaction mixture
- customthe residue triturated with ether
Sources & evidence
- ORD record
- ord-85f0a30f0f794270935a0322868da900
- Source dataset
- uspto-grants-1979_05
- Patent number
- US04156723
Reaction notes
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