Hydrochloric Acid → HCID 20706036, compound

HRID 429891Notes

Reaction equation

HRID 429891 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

5

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

  1. customTo a 500 mL 3-necked flask equipped with a magnetic stirrer and a reflux condenser
  2. customby bubbling HCl gas through for 3 min
  3. customA clear solution resulted which
  4. temperaturewas heated
  5. temperatureat reflux for 5h
  6. concentrationconcentrated in vacuo to dryness
  7. customto give a white solid
  8. washwashed with 5% aqueous NaHCO3 (4×80 mL)
  9. concentrationThe CH2Cl2 solution was concentrated to a volume of 20 mL
  10. additiondiluted to 60 mL with ethyl ether
  11. additiontreated with 16 mL of 1M ethereal HCl
  12. customA white solid precipitated which
  13. filtrationwas collected by vacuum filtration
  14. customdried in vacuo

Sources & evidence

ORD record
ord-1345ca3cee3e4f2a9a93ff16def32ea8
Source dataset
uspto-grants-2001_11
Patent number
US06319702B1

Reaction notes

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