Hydrogen Bromide → HCID 50943228, compound

HRID 1365555Notes

Reaction equation

HRID 1365555 reaction equation
C1(=O)[N:5]([CH2:6][C:7](=[O:14])[CH2:8][CH2:9][C:10]([O:12]C)=[O:11])C(=O)C2=CC=CC=C12.[BrH:21]>>[BrH:21].[NH2:5][CH2:6][C:7](=[O:14])[CH2:8][CH2:9][C:10]([OH:12])=[O:11]

Participants

3

Procedure

A stirred mixture of methyl 5-phthalimido-4-oxopentanoate (4.0 g, 14.5 mmol) [Z. Naturforsch. 41B, 1593-94 (1986)] and 48% hydrobromic acid (40 ml) was refluxed for 7 hrs, then cooled to room temperature and stored overnight in a refrigerator. Following filtering the residue was washed with water and the combined filtrates were evaporated to dryness on a rotary evaporator and titrated with diethyl ether (2×25 ml). The residue was filtered and dried over silica gel at 30° C. and 15 mm Hg in a drying pistol. The crude product was dissolved in methanol (10 ml) and 2-propanol (30 ml). Diethyl ether (150 ml) was added and the mixture was allowed to stand 2 hrs. The precipitate was filtered and dried as before, to give 2.5 g (81%), mp 137-140° C.

Workup

  1. temperaturewas refluxed for 7 hrs
  2. filtrationFollowing filtering the residue
  3. washwas washed with water
  4. customthe combined filtrates were evaporated to dryness on a rotary evaporator
  5. filtrationThe residue was filtered
  6. customdried over silica gel at 30° C.
  7. dissolutionThe crude product was dissolved in methanol (10 ml)
  8. additionDiethyl ether (150 ml) was added
  9. waitto stand 2 hrs
  10. filtrationThe precipitate was filtered
  11. customdried as before,
  12. customto give 2.5 g (81%), mp 137-140° C.

Sources & evidence

ORD record
ord-846f3b92123d466897f484326ab65d1f
Source dataset
uspto-grants-2011_02
Patent number
US07888526B2

Reaction notes

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