Potassium Bromide → Clavulanic Acid

HRID 1390935Notes

Reaction equation

HRID 1390935 reaction equation
[CH2:1]1[C:4](=[O:5])[N:3]2[C@@H:6]([C:12]([O:14]CC3C=CC=CC=3)=[O:13])/[C:7](/[O:11][C@H:2]12)=[CH:8]/[CH2:9][OH:10].C(=O)(O)[O-].[Na+].[K+].[Br-]>C(O)C.O.[Pd]>[CH2:1]1[C:4](=[O:5])[N:3]2[C@@H:6]([C:12]([OH:14])=[O:13])/[C:7](/[O:11][C@H:2]12)=[CH:8]/[CH2:9][OH:10]

Participants

7

Procedure

Benzyl clavulanate (840 mgs) in ethanol (30 ml) and water (5ml) was hydrogenated over 10% Pd/C (267 mgs) and sodium bicarbonate (244 mgs) for 25 minutes at room temperature and atmospheric pressure. The catalyst was filtered, washed with water and ethanol and the combined filtrates were evaporated in vacuo. The product crystallized from a water-acetone mixture as microneedles (565 mgs). Recrystallization from water-acetone gave needles which, after drying ever P2O5 in vacuo for 24 hours gave the following analysis: C 41.01, 40.86; H 3.77, 3.64; N 5.68, 5.51; i.r. (KBr disc) 1785, 1700, 1620 cm-1 ; Nmr (D2O) 3.06 (d,1, J=18.5Hz), 3.57 (dd,1,J1 =18.5Hz, J2 =2.5Hz), 4.15 (d,2,J=8Hz), 5.3 (HOD), 4.9(m), 5.71 (d,1,J=2.5Hz).

Workup

  1. filtrationThe catalyst was filtered
  2. washwashed with water and ethanol
  3. customthe combined filtrates were evaporated in vacuo
  4. customThe product crystallized from a water-acetone mixture as microneedles (565 mgs)
  5. customRecrystallization from water-acetone
  6. customgave needles which
  7. dry with materialafter drying ever P2O5 in vacuo for 24 hours
  8. customgave the following analysis

Sources & evidence

ORD record
ord-38d4c978e2964de4a52824e7d9d6d20c
Source dataset
uspto-grants-1979_02
Patent number
US04140764

Reaction notes

Loading…