Diketene → HCID 20379294, compound
Reaction equation
[CH2:1]=[C:2]1[O:6][C:4](=[O:5])[CH2:3]1.[NH:7]=[C:8]1[N:12]([CH3:13])[CH2:11][CH2:10][S:9]1>C(O)C>[C:4]([N:7]=[C:8]1[N:12]([CH3:13])[CH2:11][CH2:10][S:9]1)(=[O:5])[CH2:3][C:2]([CH3:1])=[O:6]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 13 g. of diketene in 100 ml. of ethanol was added dropwise to an ice-cold solution of 18 g. of 2-imino-3-methylthiazolidine in 100 ml. of ethanol. The mixture was allowed to warm spontaneously to room temperature and then evaporated to dryness. The residue was triturated with ether, collected on a filter and dried in a dessicator to give 2-acetoacetylimino-3-methylthiazolidine, m.p. 43°-45° C.
Workup
- customevaporated to dryness
- customThe residue was triturated with ether
- customcollected on
- filtrationa filter
- customdried in a dessicator
Sources & evidence
- ORD record
- ord-6148cb7146634080b4e1a465048eeb32
- Source dataset
- uspto-grants-1980_01
- Patent number
- US04181661
Reaction notes
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