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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Penten-1-OLHCID 13181—
ReactantSodium HydroxideHCID 14798—
ReactantDiisopropylethylamineHCID 81531—
ReactantTriphosgeneHCID 94429—
Reactantethyl (2S)-2-aminonon-8-enoateHCID 59493566—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl (2S)-2-{[(pent-4-en-1-yloxy)carbonyl]amino}non-8-enoateHCID 86647499122.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377874B2
Source datasetuspto-grants-2013_02
ORD IDord-9b3472f1b54542038d9f5857c636b3fe
Source noteuspto-grants-2013_02