HCID 12901511, compound → 4-[(Prop-2-en-1-yl)oxy]-2-benzofuran-1,3-dione

HRID 1105810Notes

Reaction equation

HRID 1105810 reaction equation
[CH2:1]([O:4][C:5]1[CH:13]=[CH:12][CH:11]=[C:7]([C:8]([OH:10])=O)[C:6]=1[C:14]([OH:16])=[O:15])[CH:2]=[CH2:3]>C1(C)C=CC=CC=1.C(OC(=O)C)(=O)C>[CH2:1]([O:4][C:5]1[CH:13]=[CH:12][CH:11]=[C:7]2[C:8]([O:16][C:14](=[O:15])[C:6]=12)=[O:10])[CH:2]=[CH2:3]

Participants

4

Reactant 1

HCID 12901511HCID 12901511, compound

Product 1

HCID 129015124-[(Prop-2-en-1-yl)oxy]-2-benzofuran-1,3-dione

Reagents, catalysts & solvents 2

HCID 1140TolueneSolventHCID 7918Acetic AnhydrideSolvent

Procedure

A mixture of 45.8 g of 3-allyloxy-phthalic acid in 200 ml of toluene and 25.5 ml of acetic anhydride is heated to the reflux temperature for 3 hours and then evaporated under reduced pressure. The residue is crystallised from diethyl ether and gives 3-allyloxy-phthalic anhydride; melting point 115°-117°.

Workup

  1. temperatureis heated to the reflux temperature for 3 hours
  2. customevaporated under reduced pressure
  3. customThe residue is crystallised from diethyl ether

Sources & evidence

ORD record
ord-541f6973765b40b490d3d8677a25e6ff
Source dataset
uspto-grants-1982_01
Patent number
US04310527

Reaction notes

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