Ethanolamine → HCID 87694169, compound
Reaction equation
[F:1][C:2]([F:8])([F:7])[C:3](OC)=[O:4].[CH2:9]([CH2:11][NH2:12])[OH:10].C1C=C2C(C(O)(O)C(=O)C2=CC=1)=O>>[F:1][C:2]([F:8])([F:7])[C:3]([NH2:12])=[O:4].[CH2:9]([CH2:11][NH2:12])[OH:10]Participants
4
Procedure
In a round-bottom flask, methyl trifluoroacetate (10.5 g, 81.9 mmol) was added to neat ethanolamine (4.0 g, 66 mmol) at room temperature with continuous stirring. Reaction completion was determined by the absence of ninhydrin activity. After 2 h, the reaction was concentrated by rotary evaporation and purified by distillation (11 mm Hg, b.p. 127° C.), yielding a colorless oil, 9.5 g, 93%.
Workup
- customReaction completion
- concentrationthe reaction was concentrated by rotary evaporation
- distillationpurified by distillation (11 mm Hg, b.p. 127° C.)
- customyielding a colorless oil, 9.5 g, 93%
Sources & evidence
- ORD record
- ord-b22d430e38934cc99c0add9e46c9c189
- Source dataset
- uspto-grants-2008_12
- Patent number
- US07462451B2
Reaction notes
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