Triethylamine → 3-Methanesulfonyloxy-1-(p-nitrobenzyloxycarbonyl)azetidine

HRID 891734Notes

Reaction equation

HRID 891734 reaction equation
[OH:1][CH:2]1[CH2:5][N:4]([C:6]([O:8][CH2:9][C:10]2[CH:15]=[CH:14][C:13]([N+:16]([O-:18])=[O:17])=[CH:12][CH:11]=2)=[O:7])[CH2:3]1.[CH3:19][S:20](Cl)(=[O:22])=[O:21].C(N(CC)CC)C>C(Cl)Cl>[CH3:19][S:20]([O:1][CH:2]1[CH2:5][N:4]([C:6]([O:8][CH2:9][C:10]2[CH:15]=[CH:14][C:13]([N+:16]([O-:18])=[O:17])=[CH:12][CH:11]=2)=[O:7])[CH2:3]1)(=[O:22])=[O:21]

Participants

5

Reactant 3

HCID 8471TriethylamineHCID 31297Methanesulfonyl chlorideHCID 22242749(4-Nitrophenyl)methyl 3-hydroxyazetidine-1-carboxylate

Product 1

HCID 222428573-Methanesulfonyloxy-1-(p-nitrobenzyloxycarbonyl)azetidineYield 100.1%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a solution of 3-hydroxy-1-(p-nitrobenzyloxycarbonyl)azetidine (3.52 g, 14.0 mmol) (obtained as described in Reference Example 54(1)) in methylene chloride (106 ml) were added methanesulfonyl chloride (1.19 ml, 15.4 mmol) and triethylamine (2.16 ml, 15.4 mmol) in an ice bath. After stirring the mixture in the ice bath for 10 minutes, the mixture was stirred at room temperature overnight. After checking the completion of the reaction, the reaction mixture was partitioned between ethyl acetate and saturated aqueous sodium hydrogencarbonate solution. The organic layer was washed with saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column using n-hexane:ethyl acetate (1:1→1:3) as the eluant to afford 3-methanesulfonyloxy-1-(p-nitrobenzyloxycarbonyl)-azetidine (4.63 g, yield 100%) as pale yellow crystals.

Workup

  1. customthe completion of the reaction
  2. customthe reaction mixture was partitioned between ethyl acetate and saturated aqueous sodium hydrogencarbonate solution
  3. washThe organic layer was washed with saturated aqueous sodium chloride solution
  4. dry with materialdried over anhydrous sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure
  7. customThe residue was purified by chromatography on a silica gel column

Sources & evidence

ORD record
ord-156d8f235be44e99a7333fa85c38d450
Source dataset
uspto-grants-2006_02
Patent number
US07001897B2

Reaction notes

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