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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396329Generated: November 4, 2026

Dimethyl methylphosphonate → (S)-tert-Butyl 1-(dimethoxyphosphoryl)-2-oxohex-5-en-3-ylcarbamate

https://huagongshe.com/reaction/1396329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl methylphosphonateHCID 12958—
Reactant(S)-Methyl 2-((tert-butoxycarbonyl)amino)pent-4-enoateHCID 9837499—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(S)-tert-Butyl 1-(dimethoxyphosphoryl)-2-oxohex-5-en-3-ylcarbamateHCID 8713289298%

Reaction Steps

To a solution of dimethyl methylphosphonate (15.85 mL, 148 mmol) in THF (99 mL) at −78° C. was added n-butyllithium (93 mL, 148 mmol) slowly. After addition was completed, the reaction mixture was stirred for 30 min and then a solution of (S)-methyl 2-(tert-butoxycarbonylamino)pent-4-enoate (6.8 g, 29.7 mmol) in THF (15 mL) was added slowly. Stirring was continued for another 40 min at −78° C. The reaction was then quenched by adding water and diluted with EtOAc. The organic layer was washed with 1 M HCl, saturated NaHCO3 and brine. The organic layer was then dried over MgSO4, filtered and concentrated to give a clear oil. The crude product was then purified by silica gel chromatography to give the desired product (9.3 g, 98%) as colorless oil. MS (ESI) m/z: 599.0 (M+Na)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901115B2
Source datasetuspto-grants-2014_12
ORD IDord-84528276d75e42e4b747168cac28828f
Source noteuspto-grants-2014_12