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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591276Generated: October 30, 2026

Potassium Carbonate → Di-tert-butyl (2S)-2-[(tert-butoxycarbonyl)amino]-5-[4-(2-fluoroethoxy)benzyl]-hexanedioate

https://huagongshe.com/reaction/591276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthane, 1-fluoro-2-iodo-HCID 69804—
ReactantDi-tert-butyl (2S)-2-[(tert-butoxycarbonyl)amino]-5-(4-hydroxybenzyl)hexanedioateHCID 70957101—
SolventDimethylformamideHCID 6228—
ProductDi-tert-butyl (2S)-2-[(tert-butoxycarbonyl)amino]-5-[4-(2-fluoroethoxy)benzyl]-hexanedioateHCID 70674547—

Reaction Steps

To a solution of 54 mg 1-fluoro-2-iodoethane (0.31 mmol) in N,N-dimethylformamide (10 mL) was subsequently added 101 mg potassium carbonate (0.73 mmol), followed by 100 mg di-tert-butyl (2S)-2-[(tert-butoxycarbonyl)amino]-5-(4-hydroxybenzyl)-hexanedioate (from example 12d; 0.21 mmol), and the resulting mixture was stirred for 4 h at room temperature. The mixture was then partitioned between water and ethyl acetate, the aqueous layer was than extracted with ethyl acetate again. The combined organic layers were washed with brine, dried over sodium sulfate, and evaporated. The residue was purified by preparative HPLC, method A to give 85 mg (62% purity adjusted yield) of the target compound in approx. 80% purity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238631B2
Source datasetuspto-grants-2016_01
ORD IDord-20b97811b0cf4a1aa94be980484668ed
Source noteuspto-grants-2016_01