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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009166Generated: October 30, 2026

(2S,3S)-(-)-3-tert-Butoxycarbonylamino-1,2-epoxy-4-phenylbutane → Trifluoroacetic acid

https://huagongshe.com/reaction/1009166

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2S,3S)-(-)-3-tert-Butoxycarbonylamino-1,2-epoxy-4-phenylbutaneHCID 9903372—
Reactant(4S)-6-bromo-2-methyl-2-(trifluoromethyl)chroman-4-amineHCID 67305954—
SolventEthanolHCID 702—
ProductTrifluoroacetic acidHCID 6422—
ProductHCID 86614140HCID 86614140—

Reaction Steps

A mixture of (4S)-6-bromo-2-methyl-2-(trifluoromethyl)chroman-4-amine (179 mg, 577 μmol) and tert-butyl(S)-1-((S)-oxiran-2-yl)-2-phenylethylcarbamate (198 mg, 750 μmol) in ethanol was heated at reflux for 16 h. At this point, there was still the starting amine left. An additional 1.3 eq of epoxide was added to the reaction, and continued to reflux for 6 h. The resulted mixture was concentrated and purified on Shimadzu HPLC to afford the title compound as a TFA salt. MS m/z: 573, 575.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973047B2
Source datasetuspto-grants-2011_07
ORD IDord-680613adb247428da1f07631a33013c2
Source noteuspto-grants-2011_07