HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600835Generated: October 30, 2026
Trifluoroacetic acid → HCID 57667096, compound
https://huagongshe.com/reaction/600835
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 2-Methoxypropene | HCID 8300 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 57667036 | HCID 57667036 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 57667096 | HCID 57667096 | 89% |
Reaction Steps
To a stirred solution of (S)-2,2-dimethyl-4-phenylaminomethyl-oxazolidine-3-carboxylic acid tert-butyl ester (650 mg) at r.t. in 1,2-dichloroethane (15 ml) under an argon atmosphere were added 2-methoxypropene (0.30 ml), trifluoroacetic acid (0.16 ml) and sodium triacetoxyborohydride (674 mg). The mixture was heated to 40° C. overnight. The mixture was cooled to r.t., directly adsorbed on silica gel and purified by chromatography (SiO2; gradient:cyclohexane->cyclohexane/EtOAc 7:3) to give (S)-4-[(isopropyl-phenyl-amino)-methyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (659 mg, 89%) as light yellow viscous oil. MS (ISP): 349.5 ([M+H]+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07902238B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-32363e059c7a4a23adf6d054826c7c0a |
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| Source note | uspto-grants-2011_03 |
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