Ammonia → HCID 14254895, compound
Reaction equation
C[O:2][C:3]([CH:5]1[N:9]([CH2:10][C:11]#[CH:12])[C:8](=[O:13])[CH2:7][CH2:6]1)=O.[NH3:14]>CO>[O:13]=[C:8]1[N:9]([CH2:10][C:11]#[CH:12])[CH:5]([C:3]([NH2:14])=[O:2])[CH2:6][CH2:7]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
An ice water chilled solution of 5-methoxycarbonyl-1-(2-propynyl)-2-pyrrolidinone (5.1 g) and sieve dried methanol (250 ml) was treated with anhydrous ammonia for ten minutes and was then allowed to stand overnight at ambient temperature. The solution was concentrated to afford an oil which crystallized (4.81 g). Recrystallization from 95% ethanol (20 ml) gave 3.07 g of almost colorless crystals, mp 145°-147° C.
Workup
- concentrationThe solution was concentrated
- customto afford an oil which
- customcrystallized (4.81 g)
- customRecrystallization from 95% ethanol (20 ml)
- customgave 3.07 g of almost colorless crystals, mp 145°-147° C.
Sources & evidence
- ORD record
- ord-d333edd99a664276a3dc0c579a828946
- Source dataset
- uspto-grants-1989_05
- Patent number
- US04833139
Reaction notes
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