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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1406843Generated: November 1, 2026

Trimethylsilyldiazomethane → Ethyl (S)-2-(Boc-amino)-6-diazo-5-oxohexanoate

https://huagongshe.com/reaction/1406843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyldiazomethaneHCID 167693—
Reactant1-(1,1-Dimethylethyl) 2-ethyl (2S)-5-oxo-1,2-pyrrolidinedicarboxylateHCID 5461186—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductEthyl (S)-2-(Boc-amino)-6-diazo-5-oxohexanoateHCID 8670066175%

Reaction Conditions

Temperature-78 °C

Reaction Steps

n-BuLi was added dropwise to a solution of TMSCHN2 (690 mL, 1.38 mol) in dry THF (3 L) (600 mL, 1.5 mol) at −78° C., and the mixture was stirred at −78° C. for 30 minutes. The mixture was then transferred to a solution of (S)-1-tert-butyl 2-ethyl 5-oxopyrrolidine-1,2-dicarboxylate (300 g, 1.17 mol) in dry THF (3 L) via cannula, and the mixture was stirred at −78° C. for 30 minutes. The reaction mixture was then quenched with sat. NH4Cl solution, and extracted with DCM three times. The combined organic layer was concentrated in vacuum and the crude product was purified by silica gel column chromatography (3:1 petroleum ether:EtOAc) to afford (S)-ethyl 2-((tert-butoxycarbonyl)amino)-6-diazo-5-oxohexanoate (262 g, 75%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916709B2
Source datasetuspto-grants-2014_12
ORD IDord-5f583f1e8a1542108ee88fdccb649559
Source noteuspto-grants-2014_12