Hydrochloric Acid → HCID 20706036, compound
Reaction equation
[I:1][C:2]1[CH:13]=[CH:12][CH:11]=[CH:10][C:3]=1[CH2:4][C@@H:5]([C:7]([OH:9])=[O:8])[NH2:6].Cl.[CH3:15]O>C(Cl)Cl>[I:1][C:2]1[CH:13]=[CH:12][CH:11]=[CH:10][C:3]=1[CH2:4][C@@H:5]([C:7]([O:9][CH3:15])=[O:8])[NH2:6]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a 500 mL 3-necked flask equipped with a magnetic stirrer and a reflux condenser were added 5.00 g of 2-iodo-L-phenylalanine.HCl and 100 mL of anhydrous MeOH. The mixture was stirred and acidified by bubbling HCl gas through for 3 min. A clear solution resulted which was heated at reflux for 5h. The solution was cooled to RT and concentrated in vacuo to dryness to give a white solid. The material was suspended in 120 mL of CH2Cl2 and washed with 5% aqueous NaHCO3 (4×80 mL). The CH2Cl2 solution was concentrated to a volume of 20 mL, diluted to 60 mL with ethyl ether and treated with 16 mL of 1M ethereal HCl. A white solid precipitated which was collected by vacuum filtration and dried in vacuo to afford 4.90 g (94%) of methyl 2-iodo-L-phenylalaninate.HCl m.p. 194-196° C.
Workup
- customTo a 500 mL 3-necked flask equipped with a magnetic stirrer and a reflux condenser
- customby bubbling HCl gas through for 3 min
- customA clear solution resulted which
- temperaturewas heated
- temperatureat reflux for 5h
- concentrationconcentrated in vacuo to dryness
- customto give a white solid
- washwashed with 5% aqueous NaHCO3 (4×80 mL)
- concentrationThe CH2Cl2 solution was concentrated to a volume of 20 mL
- additiondiluted to 60 mL with ethyl ether
- additiontreated with 16 mL of 1M ethereal HCl
- customA white solid precipitated which
- filtrationwas collected by vacuum filtration
- customdried in vacuo
Sources & evidence
- ORD record
- ord-1345ca3cee3e4f2a9a93ff16def32ea8
- Source dataset
- uspto-grants-2001_11
- Patent number
- US06319702B1
Reaction notes
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