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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591294Generated: November 2, 2026

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

https://huagongshe.com/reaction/591294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Iodo-3-fluoropropaneHCID 12899128—
Reactantdi-tert-butyl (4R)-N-(tert-butoxycarbonyl)-4-(4-hydroxybenzyl)-D-glutamateHCID 70957029—
SolventDimethylformamideHCID 6228—
ProductDi-tert-butyl (4R)-N-(tert-butoxycarbonyl)-4-[4-(3-fluoropropoxy)benzyl]-D-glutamateHCID 70674428—

Reaction Conditions

Temperature100 °C

Reaction Steps

To 140 mg (0.30 mmol) of di-tert-butyl (4R)—N-(tert-butoxycarbonyl)-4-(4-hydroxy-benzyl)-D-glutamate in 5 mL N,N-dimethylformamide were added 42 mg (0.3 mmol) of powdered potassium carbonate and 56 mg (0.30 mmol) of 1-iodo-3-fluoropropane (ABCR GmbH, Germany) and the resulting suspension was heated for 2 h at 100° C. in a microwave oven. The reaction mixture was then 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-21db3bd9c8204eda8ad6943dd2fd18b5
Source noteuspto-grants-2016_01