Toluene → HCID 12783486, compound
Reaction equation
[CH:1](=O)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH3:11].Cl.[NH2:14][CH2:15][CH2:16][SH:17].C1(C)C=CC=CC=1>O>[CH2:2]([CH:1]1[NH:14][CH2:15][CH2:16][S:17]1)[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH3:11]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 34 g. of undecylaldehyde and 22.8 g. of 2-aminoethanethiol hydrochloride in about 400 ml. of toluene was heated at reflux overnight. The water of condensation was collected in a Dean-Stark trap. The reaction mixture then was washed with aqueous sodium hydroxide and dried over anhydrous magnesium sulfate. After filtering the reaction mixture, the toluene was distilled under reduced pressure. The residue then was vacuum distilled, b.p. 130°-8°/0.1 mm, giving 2-decylthiazolidine. The following elemental microanalysis was obtained:
Workup
- additionA mixture of 34 g
- temperatureat reflux overnight
- customwas collected in a Dean-Stark trap
- washThe reaction mixture then was washed with aqueous sodium hydroxide
- dry with materialdried over anhydrous magnesium sulfate
- filtrationAfter filtering the reaction mixture
- distillationthe toluene was distilled under reduced pressure
- distillationdistilled
Sources & evidence
- ORD record
- ord-37360e063b4e4878bb9b3ca165f12e9b
- Source dataset
- uspto-grants-1981_09
- Patent number
- US04289766
Reaction notes
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