Ethanol → HCID 11820427, compound
Reaction equation
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]([CH:8]1OC(=O)[CH2:10][CH2:9]1)=O.[OH2:14].[NH2:15][NH2:16].[CH2:17]([OH:19])C>>[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]1[CH:8]([CH2:17][OH:19])[CH2:9][C:10](=[O:14])[NH:15][N:16]=1Participants
4
Procedure
11.8 g (0.06 mol) of 4-(2-thienyl-carbonyl)-γ-butyrolactone and 3.1 g (0.062 mol) of hydrazine hydrate are stirred in 100 ml of ethanol at room temperature for 2 hours. The precipitated hydrazone is filtered off with suction, 60 ml of toluene and 6 ml of acetic acid are added and the mixture is heated under reflux for 2 hours. After the mixture has been cooled, the precipitated product is filtered off with suction, washed and dried.
Workup
- filtrationThe precipitated hydrazone is filtered off with suction, 60 ml of toluene and 6 ml of acetic acid
- additionare added
- temperaturethe mixture is heated
- temperatureunder reflux for 2 hours
- temperatureAfter the mixture has been cooled
- filtrationthe precipitated product is filtered off with suction
- washwashed
- customdried
Sources & evidence
- ORD record
- ord-6ba4dbd5e5544135ba07533078f017a0
- Source dataset
- uspto-grants-1987_05
- Patent number
- US04666902
Reaction notes
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