HCID 13588837, compound → HCID 54395479, compound
Reaction equation
[CH2:1]([C:5]1[S:9][C:8]([CH:10]([CH2:14][C:15]([OH:17])=[O:16])[C:11]([OH:13])=O)=[CH:7][CH:6]=1)[CH:2]([CH3:4])[CH3:3]>C(Cl)(=O)C>[CH2:1]([C:5]1[S:9][C:8]([CH:10]2[CH2:14][C:15](=[O:16])[O:17][C:11]2=[O:13])=[CH:7][CH:6]=1)[CH:2]([CH3:3])[CH3:4]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
10 g of (5-isobutyl-2-thienyl)succinic acid was added to 40 cc of acetyl chloride and the mixture was refluxed for 1 hour 30 minutes. The excess acetyl chloride was evaporated under reduced pressure. Distillation of the residue provided 7.9 g (yield=85%) of (5-isobutyl-2-thienyl)succinic anhydride.
Workup
- temperaturethe mixture was refluxed for 1 hour 30 minutes
- customThe excess acetyl chloride was evaporated under reduced pressure
- distillationDistillation of the residue
Sources & evidence
- ORD record
- ord-d99d16d11ac04b1e84b12f51b7d862ad
- Source dataset
- uspto-grants-1987_03
- Patent number
- US04649153
Reaction notes
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