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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473716Generated: October 30, 2026

6-tert-Butyl 1-ethyl (E)-(S)-5-[(tert-butoxycarbonyl)amino]-2-(3-fluoropropyl)hex-2-enedioate → 1-tert-Butyl 6-ethyl (2S)-2-[(tert-butoxycarbonyl)amino]-5-(3-fluoropropyl)hexanedioate

https://huagongshe.com/reaction/1473716

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-tert-Butyl 1-ethyl (E)-(S)-5-[(tert-butoxycarbonyl)amino]-2-(3-fluoropropyl)hex-2-enedioateHCID 86678427—
Reactant6-tert-Butyl 1-ethyl (Z)-(S)-5-[(tert-butoxycarbonyl)amino]-2-(3-fluoro-propyl)hex-2-enedioateHCID 86678428—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-tert-Butyl 6-ethyl (2S)-2-[(tert-butoxycarbonyl)amino]-5-(3-fluoropropyl)hexanedioateHCID 86678429—

Reaction Steps

A mixture of 6-tert-Butyl 1-ethyl (E)-(S)-5-[(tert-butoxycarbonyl)amino]-2-(3-fluoropropyl)hex-2-enedioate and 6-tert-Butyl 1-ethyl (Z)—(S)-5-[(tert-butoxycarbonyl)amino]-2-(3-fluoro-propyl)hex-2-enedioate (100 mg, 0.25 mmol) and palladium (20.0 mg, 10% on charcoal, 0.02 mmol) in ethanol (10 mL) were stirred for 2 h at r.t. under a hydrogen atmosphere. Then the mixture was filtered through Celite® and concentrated under reduced pressure. The crude product was purified by column chromatography (silica, hexanes/ethyl acetate gradient).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09017645B2
Source datasetuspto-grants-2015_04
ORD IDord-9ce724dc86cc47d5951f70267ede7582
Source noteuspto-grants-2015_04