Isopropanol → HCID 70590458, compound

HRID 1395515Notes

Reaction equation

HRID 1395515 reaction equation
Br[CH2:2][C:3]1([CH3:29])[CH:7]([C:8]([O:10][CH2:11][C:12]([Cl:15])([Cl:14])[Cl:13])=[O:9])[N:6]2[C:16](=[O:28])[CH:17]([NH:18][C:19](=[O:27])[CH2:20][C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)[C@H:5]2[S:4]1.[CH:30]([OH:33])([CH3:32])[CH3:31]>O1CCCC1.F[B-](F)(F)F.[Ag+]>[CH3:29][C:3]1([O:33][CH:30]([CH3:32])[CH3:31])[CH:7]([C:8]([O:10][CH2:11][C:12]([Cl:15])([Cl:14])[Cl:13])=[O:9])[N:6]2[C:16](=[O:28])[CH:17]([NH:18][C:19](=[O:27])[CH2:20][C:21]3[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=3)[C@H:5]2[S:4][CH2:2]1

Participants

5

Procedure

2,2,2-Trichloroethyl 2-bromomethyl-2-methyl-6-(2-phenylacetamido)penam-3-carboxylate (0.55 g) was dissolved in a mixture of tetrahydrofuran (5 ml) and isopropanol (5 ml). To this solution was added silver fluoroborate (0.24 g) under ice-cooling and the mixture was stirred for 1 hour. The reaction mixture was concentrated and the obtained residue was dissolved in chloroform. This solution was washed with a saturated sodium bicarbonate aqueous solution and with water and then dried over magnesium sulfate. The residue obtained by distilling off the solvent was purified by chromatography on silica gel using chloroform as developing solvent to give oily 2,2,2-trichloroethyl 3-methyl-3-isopropoxy-7-(2-phenylacetamido)-cepham-4-carboxylate (0.10 g).

Workup

  1. temperaturecooling
  2. concentrationThe reaction mixture was concentrated
  3. dissolutionthe obtained residue was dissolved in chloroform
  4. washThis solution was washed with a saturated sodium bicarbonate aqueous solution and with water
  5. dry with materialdried over magnesium sulfate
  6. customThe residue obtained
  7. distillationby distilling off the solvent
  8. customwas purified by chromatography on silica gel

Sources & evidence

ORD record
ord-8d5860dde08c4f56a5552a117800ec8b
Source dataset
uspto-grants-1980_05
Patent number
US04203897

Reaction notes

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