HCID 21079761, compound → HCID 21079760, compound

HRID 1272187Notes

Reaction equation

HRID 1272187 reaction equation
[CH2:1]([C:3]1[CH:8]=[CH:7][C:6]([CH2:9][C:10]([O:12][CH2:13][CH3:14])=[O:11])=[CH:5][C:4]=1[O:15]C)[CH3:2]>C(Cl)Cl>[OH:15][C:4]1[CH:5]=[C:6]([CH2:9][C:10]([O:12][CH2:13][CH3:14])=[O:11])[CH:7]=[CH:8][C:3]=1[CH2:1][CH3:2]

Participants

3

Reactant 1

HCID 21079761HCID 21079761, compound

Product 1

HCID 21079760HCID 21079760, compoundYield 71.1%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent2×

Procedure

A solution of ethyl 4-ethyl-3-methoxyphenylacetate (4f; 3.0 g; 13.50 mmol) and CH2Cl2 (80 mL) cooled to −78° C. and a solution of (5.10 mL; 53.94 mmol; 1.0 M in CH2Cl2) over 30 min. After 1 at −78° C. the reaction was allowed to warm to rt and stirred for 12 h. The reaction was cooled in an ice-water bath and the reaction quenched with 20 mL of water. The aqueous phase was extracted with CH2Cl2:EtOAc (4:1 v/v), dried (Na2SO4), filtered and evaporated. The crude product was purified by silica gel chromatography and eluted with a CH2Cl2:EtOAc gradient (100:1→100:4) to yield 5b (2.0 g; 71%): m.s. 209.2 (M+H)+.

Workup

  1. customat −78° C.
  2. temperatureThe reaction was cooled in an ice-water bath
  3. customthe reaction quenched with 20 mL of water
  4. extractionThe aqueous phase was extracted with CH2Cl2:EtOAc (4:1 v/v)
  5. dry with materialdried (Na2SO4)
  6. filtrationfiltered
  7. customevaporated
  8. customThe crude product was purified by silica gel chromatography
  9. washeluted with a CH2Cl2

Sources & evidence

ORD record
ord-2b801a3f6eaa471bb2c41814179dde53
Source dataset
uspto-grants-2007_04
Patent number
US07208509B2

Reaction notes

Loading…