N-Hydroxysuccinimide → HCID 57824469, compound

HRID 1475134Notes

Reaction equation

HRID 1475134 reaction equation
[CH3:1][O:2][C@H:3]([C@@H:6]([C@H:9]([C@H:12]([CH3:14])[OH:13])[O:10][CH3:11])[O:7][CH3:8])[CH:4]=[O:5].O[N:16]1[C:20](=[O:21])[CH2:19][CH2:18][C:17]1=[O:22]>C1C=CC=CC=1.C1(C)C=CC(S(O)(=O)=O)=CC=1>[CH3:1][O:2][C@@H:3]1[C@H:6]([O:7][CH3:8])[C@@H:9]([O:10][CH3:11])[C@H:12]([CH3:14])[O:13][C@H:4]1[O:5][N:16]1[C:20](=[O:21])[CH2:19][CH2:18][C:17]1=[O:22]

Participants

5

Reactant 2

HCID 80170N-HydroxysuccinimideHCID 14104333HCID 14104333, compound

Product 1

HCID 57824469HCID 57824469, compoundYield 52%

Reagents, catalysts & solvents 2

HCID 6101p-Toluenesulfonic acidCatalystHCID 241BenzeneSolvent

Procedure

To a stirred solution of 2,3,4-tri-O-methyl-L-rhamnose (6.5 g, 31.5 mmol) and N-hydroxysuccinimide (5.4 g, 47 mmol) in 50 mL of benzene was added 50 mg (cat) of p-toluenesulfonic acid. The solution was heated to reflux and water was collected using a Dean-Stark trap. After 4 h, the solution was cooled and the supernatant toluene layer was separated from a small amount of insoluble gum. The organic layer was washed with 20 mL of saturated NaHCO3 solution, then dried over MgSO4 and concentrated to a solid. Recrystallization from ether-hexanes gave 4.95 g (52%) of the title compound as an off-white solid.

Workup

  1. temperatureThe solution was heated
  2. temperatureto reflux
  3. customwater was collected
  4. temperaturethe solution was cooled
  5. customthe supernatant toluene layer was separated from a small amount of insoluble gum
  6. washThe organic layer was washed with 20 mL of saturated NaHCO3 solution
  7. dry with materialdried over MgSO4
  8. concentrationconcentrated to a solid
  9. customRecrystallization from ether-hexanes

Sources & evidence

ORD record
ord-04f1e288e1184fc39e1f54b5da9f03f3
Source dataset
uspto-grants-2015_04
Patent number
US09018363B2

Reaction notes

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