Reaction #1773

ord-e05a7f6ef00b40218847ea8339f5616a

Reaction equation

O[C@@H]1CCCC[C@H]1c1ccccc1
trans-2-phenyl-1-cyclohexanol
CCOC(=O)N=NC(=O)OCC
diethyl azodicarboxylate
COC(=O)c1ccc(O)cc1OC
methyl 4-hydroxy-2-methoxybenzoate
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
COC(=O)c1ccc(OC(=O)[C@@H]2CCCC[C@@H]2c2ccccc2)cc1OC
methyl 4-(cis-2-phenyl-1-cyclohexanoyloxy)-2-methoxybenzoate

Solvents

Conditions

Temperature
0°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    FiltrationThe reaction was filtered
  2. 2
    Otherthe solvent was removed under reduced pressure
  3. 3
    OtherThe residue was chromatographed on a silica gel column
  4. 4
    WashEtOAc and eluted with same
  5. 5
    Otherthe solvent removed under reduced pressure

Procedure

To a stirred solution of methyl 4-hydroxy-2-methoxybenzoate (310 mg, 1.7 mmol) in dry THF (1.25 mL) was added triphenylphosphine (446 mg, 1.7 mmol) and the solution was cooled to 0° C. A 500 mL volume of trans-2-phenyl-1-cyclohexanol (200 mg, 1.35 mmol) and diethyl azodicarboxylate (319 μL, 2.02 mmol) in THF was added dropwise via addition funnel over 0.5 h. The reaction was filtered and the solvent was removed under reduced pressure. The residue was chromatographed on a silica gel column packed in 92:8 hexanes:EtOAc and eluted with same. The appropriate fractions were combined and the solvent removed under reduced pressure to afford methyl 4-(cis-2-phenyl-1-cyclohexanoyloxy)-2-methoxybenzoate.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05726172uspto-grants-1998_03