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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 9-Bromo-9-phenylfluorene | HCID 231624 | — |
| Reactant | (S)-Methyl 2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-hydroxypropanoate | HCID 7020783 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Nalpha-(9-fluorenylmethoxycarbonyl)-O-(9-phenyl-9H-fluoren-9-yl)-L-serine methyl ester | HCID 15516029 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06162824 |
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| Source dataset | uspto-grants-2000_12 |
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| ORD ID | ord-acb2451a8423426a847ebb7c0c5b9c6a |
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| Source note | uspto-grants-2000_12 |
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