Dodecylamine → HCID 13361730, compound
Reaction equation
O=[CH:2][C@@H:3]([C@H:5]([C@@H:7]([C@@H:9]([CH2:11][OH:12])[OH:10])[OH:8])[OH:6])[OH:4].[CH2:13]([NH2:25])[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24]>C(O)C>[CH2:13]([NH:25][C@@H:2]1[O:10][C@H:9]([CH2:11][OH:12])[C@@H:7]([OH:8])[C@H:5]([OH:6])[C@H:3]1[OH:4])[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
18 g of glucose were stirred in 50 ml of ethanol at 70° C., 18.5 g of dodecylamine were then added, the mixture was heated again until a clear solution was obtained, the solution was allowed to cool to room temperature and, after 20 hours, the crystals which had precipitated were filtered off with suction. The product was washed with ethanol and ether and dried in vacuo.
Workup
- temperaturethe mixture was heated again until a clear solution
- customwas obtained
- customthe crystals which had precipitated
- filtrationwere filtered off with suction
- washThe product was washed with ethanol and ether
- customdried in vacuo
Sources & evidence
- ORD record
- ord-94df5f7afcbe498fb9cdecc1eb1bb5a6
- Source dataset
- uspto-grants-1987_12
- Patent number
- US04710491
Reaction notes
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