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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275749Generated: October 25, 2026

Potassium Iodide → Nalpha-(9-fluorenylmethoxycarbonyl)-O-(9-phenyl-9H-fluoren-9-yl)-L-serine methyl ester

https://huagongshe.com/reaction/1275749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant9-Bromo-9-phenylfluoreneHCID 231624—
Reactant(S)-Methyl 2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-hydroxypropanoateHCID 7020783—
SolventAcetonitrileHCID 6342—
ProductNalpha-(9-fluorenylmethoxycarbonyl)-O-(9-phenyl-9H-fluoren-9-yl)-L-serine methyl esterHCID 15516029—

Reaction Conditions

Temperature40 °C

Reaction Steps

To a mixture of 0.17 g (0.5 mmol) Nα -(9-fluorenylmethoxycarbonyl)-L-serine methyl ester, 0.043 g (0.6 mmol) potassium carbonate and 0.083 g (0.5 mmol) potassium iodide in acetonitrile (2 mL) was added 0.16 g (0.5 mmol) of 9-bromo-9-phenyl-9H-fluorene (Aldrich), and the mixture stirred at 40° C. for 2 h. Filtration and removal of the solvent under vacuo gave the crude Nα -(9-fluorenylmethoxycarbonyl)-O-(9-phenyl-9H-fluoren-9-yl)-L-serine methyl ester which was subjected to the Fmoc deprotection in Step 2 without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06162824
Source datasetuspto-grants-2000_12
ORD IDord-acb2451a8423426a847ebb7c0c5b9c6a
Source noteuspto-grants-2000_12