HCID 13476626, compound → HCID 43134871, compound
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([CH3:16])([CH2:12][C:13]([OH:15])=[O:14])[C:9](O)=[O:10])=[CH:4][CH:3]=1>C(OC(=O)C)(=O)C>[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2([CH3:16])[CH2:12][C:13](=[O:15])[O:14][C:9]2=[O:10])=[CH:4][CH:3]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of the diacid prepared in Example 3 (7 g, 0.034 mole) in 18 g of acetic anhydride was refluxed for 3 hours producing a light brown solution. The reaction mixture was concentrated in vacuo to the product as a syrup. This syrupy anhydride may be used without further purification or purified by distillation.
Workup
- customproducing a light brown solution
- concentrationThe reaction mixture was concentrated in vacuo to the product as a syrup
- customThis syrupy anhydride may be used without further purification
- distillationpurified by distillation
Sources & evidence
- ORD record
- ord-e774029532404b3c826059a9bce9e2b5
- Source dataset
- uspto-grants-1985_06
- Patent number
- US04524206
Reaction notes
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