Water → HCID 59587910, compound

HRID 1808908Notes

Reaction equation

HRID 1808908 reaction equation
[CH3:1][O:2][C:3]1[CH:14]=[CH:13][C:6]([CH2:7][N:8]2[CH2:12][CH:11]=[CH:10][CH2:9]2)=[CH:5][CH:4]=1.O.[OH:16]S(O)(=O)=O.ClC1C=C(C=CC=1)C(OO)=O>CO.C(OCC)(=O)C.CCCCCC.C(OCC)(=O)C>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([CH2:7][N:8]2[CH2:12][CH:11]3[CH:10]([O:16]3)[CH2:9]2)=[CH:13][CH:14]=1

Participants

8

Procedure

To a solution of 4-methoxybenzyl-3-pyrroline (3.0 g, 15.8 mmol) in methanol (12 ml) cooled at 0° C., water was added (3 ml) and H2SO4 96% (1.0 ml, 19.0 mmol). The solution was stirred for 10 min. and 3-chloroperoxybenzoic acid (5.0 g, 20.5 mmol) was added in portions. The suspension was stirred at room temperature for 18 hours. Methanol was evaporated, water (15 ml) was added and the aqueous solution was neutralized with aq. NaOH 20% until pH=7. The suspension was extracted with dichloromethane and the organic phase was washed with saturated solution of NaHCO3, water and saturated solution of NaCl, dried over Na2SO4, filtered and concentrated. The residue was purified by flash chromatography: silica gel, gradient hexane:ethyl acetate (1:1) to neat ethyl acetate to give the titled compound (1.92 g, 59% yield) as yellow oil.

Workup

  1. stirringThe suspension was stirred at room temperature for 18 hours
  2. customMethanol was evaporated
  3. additionwater (15 ml) was added
  4. extractionThe suspension was extracted with dichloromethane
  5. washthe organic phase was washed with saturated solution of NaHCO3, water and saturated solution of NaCl
  6. dry with materialdried over Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customThe residue was purified by flash chromatography

Sources & evidence

ORD record
ord-05e6cb8015474485adf6ee54cc380b7b
Source dataset
uspto-grants-2013_01
Patent number
US08362011B2

Reaction notes

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