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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl methylphosphonate | HCID 12958 | — |
| Reactant | (S)-Methyl 2-((tert-butoxycarbonyl)amino)pent-4-enoate | HCID 9837499 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-tert-Butyl 1-(dimethoxyphosphoryl)-2-oxohex-5-en-3-ylcarbamate | HCID 87132892 | 98% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08901115B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-84528276d75e42e4b747168cac28828f |
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| Source note | uspto-grants-2014_12 |
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