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 are stirred in 50 ml of ethanol at 70° C., then 18.5 g of dodecylamine are added, heating is continued until a clear solution is obtained, and this is allowed to cool to room temperature and, after 20 hours, the crystals which have separated out are filtered off with suction. They are washed with ethanol and ether and dried in vacuo.
Workup
- temperatureheating
- customis obtained
- customthe crystals which have separated out
- filtrationare filtered off with suction
- washThey are washed with ethanol and ether
- customdried in vacuo
Sources & evidence
- ORD record
- ord-0930781d79974684be016b8bbf67121b
- Source dataset
- uspto-grants-1987_07
- Patent number
- US04680287
Reaction notes
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