HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2169181Generated: October 25, 2026
Ethanolamine → Oxazolidine, 2-methyl-2-(trifluoromethyl)-
https://huagongshe.com/reaction/2169181
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Methyl trifluoromethyl ketone | HCID 9871 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Oxazolidine, 2-methyl-2-(trifluoromethyl)- | HCID 43316684 | 60.8% |
Reaction Steps
A solution of 2-aminoethanol (10.15 g, 10.0 ml, 166 mmol, Eq: 1.00) in dichloromethane (250 ml) was cooled to −30° C. and stirred while 1,1,1-trifluoropropan-2-one (20.1 g, 16.1 ml, 179 mmol, Eq: 1.08), followed by molecular sieves (4 Å, powder <5 micron, activated; 20.0 g, 166 mmol, Eq: 1.00) were added. The mixture was stirred at −30° C. for 3 h and then allowed to warm to room temperature and left stirring for overnight. The mixture was filtered, washed with dichloromethane, and concentrated to obtain 2-methyl-2-(trifluoromethyl)oxazolidine (39) (oil, 15.60 g, 101 mmol, 60.5% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09045486B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-f0181f17c1d0418ca29c1159c57a4a8e |
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| Source note | uspto-grants-2015_06 |
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