Octadecylamine → N-octadecylglucopyranosylamine

HRID 482669Notes

Reaction equation

HRID 482669 reaction equation
[CH2:1]([NH2:19])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18].[O:20]=[CH:21][C@@H:22]([C@H:24]([C@@H:26]([C@@H:28]([CH2:30][OH:31])[OH:29])[OH:27])[OH:25])O>C(O)C>[CH2:1]([NH:19][CH:30]1[O:31][C@H:22]([CH2:21][OH:20])[C@@H:24]([OH:25])[C@H:26]([OH:27])[C@H:28]1[OH:29])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18]

Participants

4

Conditions

Temperature
70 °C

Procedure

20 g of octadecylamine are dissolved in 120 ml of ethanol and the solution is warmed to 70° C. 11 g of anhydrous D-glucose are added. Stirring is continued for a further 15 minutes at 70° after a clear solution has been formed. The mixture is cooled to 10° and allowed to stand for 15 minutes. The resulting mash of crystals is filtered off with suction, washed twice with ethanol and dried in vacuo.

Workup

  1. customafter a clear solution has been formed
  2. temperatureThe mixture is cooled to 10°
  3. waitto stand for 15 minutes
  4. filtrationThe resulting mash of crystals is filtered off with suction
  5. washwashed twice with ethanol
  6. customdried in vacuo

Sources & evidence

ORD record
ord-f5c1083aeef2444aa9e5e69943a81c6f
Source dataset
uspto-grants-1986_03
Patent number
US04574122

Reaction notes

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