Hydrochloric Acid → 16-Aminohexadecan-1-ol
Reaction equation
COC[O: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][CH2:18][CH2:19][CH2:20][NH2:21].Cl>CO>[NH2:21][CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][OH:4]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a suspension of 0.65 g of 16-methoxymethoxyhexadecylamine in 40 ml of methanol was added 1 ml of conc. hydrochloric acid and the mixture was heated under reflux for one hour. The reaction solution was distilled under reduced pressure. The residue was diluted with a 1N aqueous solution of sodium hydroxide, extracted with chloroform, dried over anhydrous sodium sulfate and distilled under reduced pressure to afford the title compound as a colorless crystal.
Workup
- temperaturethe mixture was heated
- temperatureunder reflux for one hour
- distillationThe reaction solution was distilled under reduced pressure
- additionThe residue was diluted with a 1N aqueous solution of sodium hydroxide
- extractionextracted with chloroform
- dry with materialdried over anhydrous sodium sulfate
- distillationdistilled under reduced pressure
Sources & evidence
- ORD record
- ord-77dc99d637e049c98f478aeb8dc0d2aa
- Source dataset
- uspto-grants-1999_10
- Patent number
- US05972943
Reaction notes
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