2,2-Diethoxyethylamine → HCID 10805622, compound
Reaction equation
[CH2:1]([O:3][CH:4]([O:7][CH2:8][CH3:9])[CH2:5][NH2:6])[CH3:2].[F:10][C:11]([F:22])([F:21])[C:12]1[CH:17]=[CH:16][C:15]([N:18]=[C:19]=[O:20])=[CH:14][CH:13]=1>>[CH2:1]([O:3][CH:4]([O:7][CH2:8][CH3:9])[CH2:5][NH:6][C:19]([NH:18][C:15]1[CH:14]=[CH:13][C:12]([C:11]([F:10])([F:21])[F:22])=[CH:17][CH:16]=1)=[O:20])[CH3:2]Participants
3
Procedure
To aminoacetoaldehyde diethylacetal (7.8 ml, 53.6 mmol) was added dropwise 10 g (53.4 mmol) of 4-trifluoromethylphenylisocyanate at 0° C. during five minutes. The reaction solution was stirred for one hour at room temperature. The crystals thus produced was collected by filtration and washed with hexane to give 16.2 g of 1-(2,2-diethoxyethyl)-3-(4-trifluoromethylphenyl)urea (95%) as a colorless powder.
Workup
- customThe crystals thus produced
- filtrationwas collected by filtration
- washwashed with hexane
Sources & evidence
- ORD record
- ord-94b780b9213441dcbb261cf2e1bcc0a9
- Source dataset
- uspto-grants-1995_11
- Patent number
- US05466820
Reaction notes
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