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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591256Generated: October 30, 2026

Potassium Carbonate → Di-tert-butyl (4S)-N-(tert-butoxycarbonyl)-4-[4-(3-fluoropropoxy)benzyl]-L-glutamate

https://huagongshe.com/reaction/591256

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Iodo-3-fluoropropaneHCID 12899128—
Reactantdi-tert-butyl (4S)-N-(tert-butoxycarbonyl)-4-(4-hydroxybenzyl)-L-glutamateHCID 70957078—
SolventDimethylformamideHCID 6228—
ProductDi-tert-butyl (4S)-N-(tert-butoxycarbonyl)-4-[4-(3-fluoropropoxy)benzyl]-L-glutamateHCID 70674426—

Reaction Conditions

Temperature60 °C

Reaction Steps

To 93 mg (0.20 mmol) of di-tert-butyl (4S)—N-(tert-butoxycarbonyl)-4-(4-hydroxybenzyl)-L-glutamate (Example 1b) in 9 mL N,N-dimethylformamide were added 60.7 mg (0.44 mmol) of powdered potassium carbonate and 45 mg (0.24 mmol) of 1-iodo-3-fluoropropane (ABCR GmbH, Germany) and the resulting suspension was stirred for 5 h at 60° C. and overnight at room temperature. The reaction mixture was than filtered, the solvent evaporated and the residue was taken up in ethyl acetate and water. The organic phase was separated off, washed with water until neutral, dried over sodium sulfate and filtered, and the filtrate was concentrated in vacuo. The crude product obtained in this manner was chromatographed on silica gel using a dichloromethane/methanol gradient, and the appropriate fractions were combined and concentrated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238631B2
Source datasetuspto-grants-2016_01
ORD IDord-82c6a512333d4a8daa38c41fb2626900
Source noteuspto-grants-2016_01