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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 24684Generated: October 29, 2026

Ethanol → N-(9-fluorenylmethoxycarbonyl)-3-(5-bromo-2-thienyl)-L-alanine ethyl ester

https://huagongshe.com/reaction/24684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantFmoc-L-2-(5-bromothienyl)alanineHCID 7006538—
ProductN-(9-fluorenylmethoxycarbonyl)-3-(5-bromo-2-thienyl)-L-alanine ethyl esterHCID 54001394—

Reaction Conditions

Temperature50 °C

Reaction Steps

N-(9-Fluorenylmethoxycarbonyl)-3-(5-bromo-2-thienyl)-L-alanine (813 mg) was dissolved in EtOH (15 mL) and HCl (gas) was bubbled through the solution for 5 min at 0° C. The mixture was warmed to 50° C. and stirred for 1 h. After cooling to room temperature the solvent was evaporated. The residue was purified by column chromatography (silica gel; eluent: hexane to hexane/EtOAc 1:1) provided N-(9-fluorenylmethoxycarbonyl)-3-(5-bromo-2-thienyl)-L-alanine ethyl ester (767 mg): ESMS: m/z 500 MH+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06855843B2
Source datasetuspto-grants-2005_02
ORD IDord-2d75f7c58b0e4ea5b2a82a14bdb9a0a0
Source noteuspto-grants-2005_02