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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444578Generated: October 26, 2026

Nitrogen → 2(S)-Boc-amino-1-(5-methoxymethyl-1,3,4-oxadiazol-2-yl)-1-butanol

https://huagongshe.com/reaction/1444578

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantDiethyl EtherHCID 3283—
Reactant2-(Methoxymethyl)-1,3,4-oxadiazoleHCID 21962688—
Reactant(S)-2-Boc-aminobutyraldehydeHCID 86590935—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2(S)-Boc-amino-1-(5-methoxymethyl-1,3,4-oxadiazol-2-yl)-1-butanolHCID 69451144—

Reaction Conditions

Temperature-45 °C

Reaction Steps

To a stirred solution of 2-methoxymethyl-1,3,4-oxadiazole (4.6 g, 40 mmol) in THF (100 mL) was added n-BuLi (1.6 M solution in 25.2 mL of hexane) dropwise under N2 at −78° C. After 1 h, MgBr.Et2O (10.4 g, 40.3 mmol) was added and the reaction mixture was allowed to warm to −45° C. for 1 h before being treated with 2(S)-Boc-aminobutyraldehyde (5.28 g, 28.25 mmol) in THF (20 mL). The reaction mixture was stirred for 1 h, quenched with saturated NH4Cl, and extracted with ethyl acetate. The organic layer was washed with brine, dried with MgSO4 and concentrated. The residue was purified by silica gel column chromatography to yield 2(S)-Boc-amino-1-(5-methoxymethyl-[1.3.4]-oxadiazol-2-yl)-1-butanol (500 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662849B2
Source datasetuspto-grants-2010_02
ORD IDord-ca32d1f6ad58478da574c924ebdf1e6a
Source noteuspto-grants-2010_02