Diethyl Ether → Methyl bicyclo[2.2.1]hept-5-ene-2-carboxylate

HRID 255948

Reaction equation

HRID 255948 reaction equation
[CH:1]1[CH2:5][CH:4]=[CH:3][CH:2]=1.[C:6]([O:10][CH3:11])(=[O:9])C=C.[CH3:12][CH2:13]OCC>>[CH:2]12[CH2:1][CH:5]([CH:12]=[CH:13]1)[CH2:4][CH:3]2[C:6]([O:10][CH3:11])=[O:9]

Participants

4

Procedure

In 100 ml of anhydrous ether at 0° C. is mixed 30 ml of cyclopentadiene and 32 ml of methyl acrylate. The ice bath is removed and the mixture allowed to stir overnight. The solvent, unreacted methyl acrylate, and cyclopentadiene are removed at ambient temperature at reduced pressure; as less material distilled out of the mixture the pressure is gradually reduced to 0.5 mm. The desired epimeric mixture of methyl carboxylates is distilled at 42°-43° and 0.5 mm; ir: 3118, 3060, 2965, 2941, 2862, 1734, 1428, 1329, 1264, 1190, 1024, 704, cm-1 ; 60 MHz NMR: endo/exo=80/20.

Workup

  1. customThe ice bath is removed
  2. customThe solvent, unreacted methyl acrylate, and cyclopentadiene are removed at ambient temperature at reduced pressure
  3. distillationas less material distilled out of the mixture the pressure
  4. additionThe desired epimeric mixture of methyl carboxylates
  5. distillationis distilled at 42°-43°

Sources & evidence

ORD record
ord-1400422becca49a1bb6736325ef80823
Source dataset
uspto-grants-1987_10
Patent number
US04699963

Linked notes

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