2-Benzylacrylic Acid → Methyl 2-benzylprop-2-enoate

HRID 1379375Notes

Reaction equation

HRID 1379375 reaction equation
[CH2:1]([C:8](=[CH2:12])[C:9]([OH:11])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:13]([O-])(O)=O.[Na+]>CO>[CH2:1]([C:8](=[CH2:12])[C:9]([O:11][CH3:13])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

4

Procedure

a-Benzylacrylic acid (1.00 g, 6.17 mmol) in methanol (20 ml) was treated with BF3 ·Et2O (2 ml). The mixture was heated to reflux for 14 h, cooled, and poured into saturated NaHCO3 solution. Extraction with ether followed by drying over Na2SO4 and evaporation afforded 1.03 g (95%) of a mobile oil. 1H NMR (CDCl3) δ 7.17-7.35 (m, 5H), 6.23 (m, 1H), 5.47 (m, 1H), 3.74 (s, 3H), 3.63 (s,2H).

Workup

  1. temperatureThe mixture was heated
  2. temperatureto reflux for 14 h
  3. temperaturecooled
  4. extractionExtraction with ether
  5. dry with materialby drying over Na2SO4 and evaporation

Sources & evidence

ORD record
ord-a7c96f3aae494019b2746bff06ea5e9d
Source dataset
uspto-grants-1997_09
Patent number
US05670675

Reaction notes

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