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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803469Generated: October 31, 2026

trimethylphosphine THF → (1R,2R,3R,5R,6R)-2-amino-3-(3,4-dichlorobenzyloxy)-6-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid 6-(2-aminoethyl)ester

https://huagongshe.com/reaction/1803469

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttrimethylphosphine THFHCID 86589763—
Reactant(1R,2R,3R,5R,6R)-2-amino-3-(3,4-dichlorobenzyloxy)-6-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid 6-(2-azidoethyl)esterHCID 86610093—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(1R,2R,3R,5R,6R)-2-amino-3-(3,4-dichlorobenzyloxy)-6-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid 6-(2-aminoethyl)esterHCID 6662858135.4%

Reaction Steps

20 μL of a 1M trimethylphosphine/tetrahydrofuran solution was added to 6 mg of (1R,2R,3R,5R,6R)-2-amino-3-(3,4-dichlorobenzyloxy)-6-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid 6-(2-azidoethyl) ester dissolved in a mixture of 0.15 mL of tetrahydrofuran and 0.02 mL of water at room temperature, and the mixture was stirred for 13 hours. After the solvent was distilled under reduced pressure, the residue was purified by reverse phase column chromatography (Wako gel 50C18 (made by Wako Pure Chemical Industries Ltd.), eluent: water to a 50% aqueous solution of acetonitrile), and the obtained solids were further washed with tetrahydrofuran, thereby yielding 2 mg of (1R,2R,3R,5R,6R)-2-amino-3-(3,4-dichlorobenzyloxy)-6-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid 6-(2-aminoethyl)ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08350060B2
Source datasetuspto-grants-2013_01
ORD IDord-042249e7216a47579d0f62148c807cd2
Source noteuspto-grants-2013_01