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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20058Generated: October 27, 2026

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

https://huagongshe.com/reaction/20058

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 numberUS07745484B2
Source datasetuspto-grants-2010_06
ORD IDord-0737efb85022439ba9ec17ec97424d0a
Source noteuspto-grants-2010_06