4-Toluenesulfonyl chloride → 3-[(tert-Butoxycarbonyl)amino]propyl 4-methylbenzene-1-sulfonate

HRID 2084595Notes

Reaction equation

HRID 2084595 reaction equation
[C:1]([O:5][C:6]([NH:8][CH2:9][CH2:10][CH2:11][OH:12])=[O:7])([CH3:4])([CH3:3])[CH3:2].C(N(CC)CC)C.[S:20](Cl)([C:23]1[CH:29]=[CH:28][C:26]([CH3:27])=[CH:25][CH:24]=1)(=[O:22])=[O:21]>C(Cl)Cl>[S:20]([C:23]1[CH:29]=[CH:28][C:26]([CH3:27])=[CH:25][CH:24]=1)([O:12][CH2:11][CH2:10][CH2:9][NH:8][C:6]([O:5][C:1]([CH3:4])([CH3:3])[CH3:2])=[O:7])(=[O:22])=[O:21]

Participants

5

Procedure

3-t-Butoxycarbonylaminopropanol (10.0 g) is dissolved in methylene chloride (100 ml) and thereto are added triethylamine (8.66 g) and tosyl chloride (16.3 g) with stirring under ice cooling. The mixture is stirred at room temperature overnight. The reaction mixture is concentrated and the residue is dissolved in water-ethyl acetate, and the organic layer is separated, washed with an aqueous saturated saline solution, dried over sodium sulfate, and then distilled off the solvent. The residue is purified with a silica gel column chromatography to give 3-t-butoxycarbonylaminopropyl tosylate (15.37 g) as pale yellow oil.

Workup

  1. stirringThe mixture is stirred at room temperature overnight
  2. concentrationThe reaction mixture is concentrated
  3. dissolutionthe residue is dissolved in water-ethyl acetate
  4. customthe organic layer is separated
  5. washwashed with an aqueous saturated saline solution
  6. dry with materialdried over sodium sulfate
  7. distillationdistilled off the solvent
  8. customThe residue is purified with a silica gel column chromatography

Sources & evidence

ORD record
ord-d2538baefe51434e82388829d1d4ed7a
Source dataset
uspto-grants-2004_04
Patent number
US06716983B2

Reaction notes

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