HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39270Generated: October 24, 2026
Nalpha-(9-fluorenylmethoxycarbonyl)-Nepsilon-(4,4-bis(diallylphosphoryl)butyryl)-L-lysine → Nepsilon-(4,4-bis(diallylphosphoryl)butyryl)-L-lysine
https://huagongshe.com/en/reaction/39270
Participants
| Role | Name | HCID | Charge |
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| Reactant | Nalpha-(9-fluorenylmethoxycarbonyl)-Nepsilon-(4,4-bis(diallylphosphoryl)butyryl)-L-lysine | HCID 86762028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | piperidine N,N-dimethylformamide | HCID 23501187 | — |
| Product | Nepsilon-(4,4-bis(diallylphosphoryl)butyryl)-L-lysine | HCID 86762027 | 85.6% |
Reaction Steps
A solution of 90 (502 mg, 0.616 mmol) in piperidine/DMF (0.05:1, 5 mL) was stirred at room temperature for 18 hr. After diluting with ethyl acetate (40 mL) the organic layer was washed with water and brine then dried over Na2SO4 and concentrated in vacuo. The crude material was purified by silica gel chromatography (methanol in ethyl acetate, 5% over 5 column volumes then 5 to 30% over 10 column volumes) using a Biotage Horizon™ apparatus resulting in the colourless liquid 91 (249 mg, 68%): 1H NMR (400 MHz, CDCl3) δ 1.39-1.74 (m, 6H), 1.45 (s, 9H), 2.21-2.35 (m, 2H), 2.51 (t, J=7.4, 2H), 2.55 (tt, J=6.9, 23.9, 1H), 3.19-3.25 (m, 2H), 3.29 (dd, J=5.2, 7.6, 1H), 4.58-4.63 (m, 8H), 5.25 (dq, J=1.3, 10.3, 4H), 5.38 (dq, J=1.4, 17.1, 4H), 5.90-6.00 (m, 4H), 6.14 (bd, J=4.9, 1H): 31P (162 MHz, CDCl3) δ 24.67 (s, 2P).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524691B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-9ace8feb681144c797b9b24e1829a87f |
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| Source note | uspto-grants-2013_09 |
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