Hydrochloric Acid → Methyl tryptophanate hydrochloride
Reaction equation
[ClH:1].[NH2:2][C@H:3]([C:14]([OH:16])=[O:15])[CH2:4][C:5]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[NH:7][CH:6]=1.[CH3:17]COCC>CO>[ClH:1].[CH3:17][O:15][C:14](=[O:16])[C@H:3]([CH2:4][C:5]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[NH:7][CH:6]=1)[NH2:2]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 20 °C
Procedure
A 1.2 M solution of HCl in MeOH (440 mL; 0.528 mol) was added to a suspension of L-tryptophan (commercial product) (30.6 g; 150 mmol) in MeOH (70 mL). The resulting clear solution was stirred for 5 days at 20° C. The solution was concentrated (35° C.; 1.3 kPa) to yield a solid which was dissolved in MeOH (10 mL). Et2O (300 mL) was added to the solution and the mixture was vigorously stirred for 1 h. The mixture was filtered and the solid was washed with Et2O (70 mL). The combined solutions were concentrated (35° C.; 1.3 kPa) to a volume of 100 mL and filtered. The solid materials were combined and dried (40° C.; P205; 1.3 kPa) to give as a white solid the desired product (38.5 g; 149.5 mmol). Quantitative yield.
Workup
- concentrationThe solution was concentrated (35° C.; 1.3 kPa)
- customto yield a solid which
- stirringthe mixture was vigorously stirred for 1 h
- filtrationThe mixture was filtered
- washthe solid was washed with Et2O (70 mL)
- concentrationThe combined solutions were concentrated (35° C.; 1.3 kPa) to a volume of 100 mL
- filtrationfiltered
- customdried (40° C.; P205; 1.3 kPa)
Sources & evidence
- ORD record
- ord-5734a32802be4445a50ef87ac719a75c
- Source dataset
- uspto-grants-2002_10
- Patent number
- US06458337B1
Reaction notes
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