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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 2-(Methoxymethyl)-1,3,4-oxadiazole | HCID 21962688 | — |
| Reactant | (S)-2-Boc-aminobutyraldehyde | HCID 86590935 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2(S)-Boc-amino-1-(5-methoxymethyl-1,3,4-oxadiazol-2-yl)-1-butanol | HCID 69451144 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07662849B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-ca32d1f6ad58478da574c924ebdf1e6a |
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| Source note | uspto-grants-2010_02 |
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