HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389177Generated: October 26, 2026
4-Penten-1-OL → Ethyl (2S)-2-{[(pent-4-en-1-yloxy)carbonyl]amino}non-8-enoate
https://huagongshe.com/reaction/389177
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Penten-1-OL | HCID 13181 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | ethyl (2S)-2-aminonon-8-enoate | HCID 59493566 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Ethyl (2S)-2-{[(pent-4-en-1-yloxy)carbonyl]amino}non-8-enoate | HCID 86647499 | 122.3% |
Reaction Steps
To a stirred solution of pent-4-en-1-ol (0.62 g, 7.21 mmol) and DIPEA (1.26 mL, 7.21 mmol) in anhydrous 1,4-dioxane (20 ml), at 10° C. and under nitrogen, was slowly added a solution of triphosgene (0.75 g, 2.52 mmol) in anhydrous 1,4-dioxane (20 mL). The reaction mixture was stirred at RT for 1 hour, and ethyl (2S)-2-aminonon-8-enoate*HCl (0.85 g, 3.61 mmol) and 1 M aqueous NaOH (7.21 ml, 7.21 mmol) added, and the reaction mixture was heated to 50° C. for 15 hours. After cooling to RT, the reaction mixture was basified to pH 8 with 1M aqueous NaOH and extracted with ether (3×200 ml). The combined organic phases were washed with water (100 mL), brine (50 mL), dried over Na2SO4, filtered and concentrated. The residue was chromatographed on silica gel (5 to 75% EtOAc in hexane) to give the title compound (0.96 g). LRMS (ESI) m/z 312.5 [(M+H)+; calcd for C17H30NO4: 312.2].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08377874B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-9b3472f1b54542038d9f5857c636b3fe |
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| Source note | uspto-grants-2013_02 |
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