Pyridine → Methyl 4-(2-oxiranylmethoxy)benzeneacetate

HRID 1385837Notes

Reaction equation

HRID 1385837 reaction equation
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([O:11][CH3:12])=[O:10])=[CH:4][CH:3]=1.[CH2:13]([CH:15]1[O:17][CH2:16]1)Cl.N1C=CC=CC=1>>[O:17]1[CH2:16][CH:15]1[CH2:13][O:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][C:9]([O:11][CH3:12])=[O:10])=[CH:6][CH:7]=1

Participants

4

Reactant 3

HCID 1049PyridineHCID 7835EpichlorohydrinHCID 518900Benzeneacetic acid, 4-hydroxy-, methyl ester

Product 1

HCID 12941054Methyl 4-(2-oxiranylmethoxy)benzeneacetate

Conditions

Temperature
85 °C

Procedure

A mixture of methyl 4-hydroxyphenylacetate (4.98 g, 0.030 mol), epichlorohydrin (23.5 ml, 0.30 mol) and pyridine (121 μl, 1.5 mmol) was stirred at 85° C. for 2 hours. The reaction mixture was cooled and excess epichlorohydrin was distilled off (rotavapor). The residue was taken up in ethyl acetate, washed with brine and dried (Na2SO4). The solution was filtered and concentrated. The dark residue was chromatographed (silica, hexane/ethyl acetate 7:3) to give 2.25 g (34 μ) of a colourless oil. 1H (300 MHz) and 13C NMR (75 MHz) spectra were in accordance with the structure.

Workup

  1. temperatureThe reaction mixture was cooled
  2. distillationexcess epichlorohydrin was distilled off (rotavapor)
  3. washwashed with brine
  4. dry with materialdried (Na2SO4)
  5. filtrationThe solution was filtered
  6. concentrationconcentrated
  7. customThe dark residue was chromatographed (silica, hexane/ethyl acetate 7:3)
  8. customto give 2.25 g (34 μ) of a colourless oil

Sources & evidence

ORD record
ord-4a7eb04b03484b0c842ad1190d4ae482
Source dataset
uspto-grants-2001_07
Patent number
US06264917B1

Reaction notes

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