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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910471Generated: November 3, 2026

HCID 82481672, compound → HCID 86687869, compound

https://huagongshe.com/reaction/1910471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 82481672HCID 82481672—
ReactantHCID 178451183HCID 178451183—
CatalystHCID 178418851HCID 178418851—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86687869HCID 8668786952.8%

Reaction Steps

To a solution of 5-(3-bromobenzyl)-3-methyl-1,2,4-oxadiazole 1098 (0.50 g, 1.97 mmol) in dioxane (1 mL), under an atmosphere of Argon, was added Bis(tri-t-butylphosphine)palladium(0) (0.15 g, 0.295 mmol) followed by the addition of 2-tert-butoxy-2-oxoethylzinc chloride (0.5 M in diethyl ether, 4.92 mmol, 9.84 mL). The mixture was allowed to stir under argon for 20 hours and the volatiles were removed under reduced pressure. The residue was taken up in EtOAc (10 mL) and washed with water (2×5 mL), brine (2×5 mL) and dried over Na2SO4. The Na2SO4 was removed by filtration and the volatiles removed under reduced pressure. The crude material was purified by normal phase chromatography 0-50% EtOAc/Hexanes to give 0.300 g tert-butyl 2-(3-((3-methyl-1,2,4-oxadiazol-5-yl)methyl)phenyl)acetate 1099. 1H NMR 300 MHz CDCl3: δ 7.40-7.18 (m, 4H), 4.17 (s, 2H), 3.51 (s, 2H), 2.36 (s, 3H), 1.43 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604016B2
Source datasetuspto-grants-2013_12
ORD IDord-7956202c5ef24597924a0b1d803551f8
Source noteuspto-grants-2013_12