Dodecylamine → HCID 86742100, compound
Reaction equation
[C:1]([NH:4][C@@H:5]1[C@@H:11]([OH:12])[C@H:10]([OH:13])[C@@H:9]([CH2:14][OH:15])[O:8][CH:6]1O)(=[O:3])[CH3:2].[CH2:16]([NH2:28])[CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH3:27]>C(O)C>[C:1]([NH:4][C@@H:5]1[C@@H:11]([OH:12])[C@H:10]([OH:13])[C@@H:9]([CH2:14][OH:15])[O:8][CH:6]1[CH2:27][CH2:26][CH2:25][CH2:24][CH2:23][CH2:22][CH2:21][CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][NH2:28])(=[O:3])[CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
15 g of N-acetylglucosamine and 19 g of dodecylamine are heated at 80° C. for 3 hours in 50 ml of ethanol, with stirring. The undissolved material is then filtered off hot, the filtrate is cooled and the precipitated product is filtered off with suction and rinsed with ethanol and ether. The residue on the filter is dried in vacuo.
Workup
- filtrationThe undissolved material is then filtered off hot
- temperaturethe filtrate is cooled
- filtrationthe precipitated product is filtered off with suction
- washrinsed with ethanol and ether
- customThe residue on the filter is dried in vacuo
Sources & evidence
- ORD record
- ord-e985ae15e7b4405a8800e94f0ad0ca48
- Source dataset
- uspto-grants-1988_04
- Patent number
- US04737488
Reaction notes
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