HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633706Generated: October 30, 2026
Methyl trifluoromethyl ketone → HCID 67776705, compound
https://huagongshe.com/reaction/633706
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl trifluoromethyl ketone | HCID 9871 | — |
| Reactant | 2-Amino-2-phenylethanol | HCID 92466 | — |
| Reactant | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 67776705 | HCID 67776705 | 84.3% |
Reaction Steps
25 g (180 mmol) of (R)-phenylglycinol and then 4 g (16 mmol) of pyridinium para-toluenesulfonate are added to a solution of 25.8 g (230 mmol) of trifluoroacetone in 200 mL of toluene in a three-necked flask on which is mounted Dean-Stark apparatus. The mixture obtained is then heated at 110° C. for 5 hours. After cooling, the reaction mixture is concentrated under reduced pressure. The residue obtained is purified by filtration on silica (eluent: dichloromethane) to give 35.10 g of (R)-2-methyl-4-phenyl-2-trifluoromethyloxazolidine in the form of a colorless liquid, the characteristics of which are as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09321790B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-0bb3c6082a2841f4adabfc6e5f59170e |
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| Source note | uspto-grants-2016_04 |
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