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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551699Generated: November 1, 2026

Allyl bromide → HCID 67197848, compound

https://huagongshe.com/reaction/551699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantTetrahydrofuranHCID 8028—
ReactantEthyl cyclobutylacetateHCID 14322004—
ReactantHCID 131728924HCID 131728924—
SolventWaterHCID 962—
ProductHCID 67197848HCID 67197848—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A 1.9 M tetramethyldisilazane sodium-tetrahydrofuran solution (9.44 mL, 18.0 mmol) was added dropwise over 10 minutes to a tetrahydrofuran (40 mL) solution of ethyl 2-cyclobutylacetate (2.32 g, 16.3 mmol) cooled to −78° C., and the mixture was then stirred at −78° C. for 10 minutes. Subsequently, a tetrahydrofuran (10 mL) solution of allyl bromide (7.90 g, 65.3 mmol) was added dropwise thereto over 10 minutes, and the mixture was stirred at room temperature for 17 hours. The mixture was treated with water, and volatile portions were then removed under reduced pressure. To the obtained liquid, ethyl acetate and water were added, and the obtained organic layer was dried over anhydrous magnesium sulfate. Then, the solvent was distilled off under reduced pressure to obtain the compound of interest as a yellow oil substance (1.80 g, 61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947738B2
Source datasetuspto-grants-2011_05
ORD IDord-99f6bc43bbdd4fb7b54f431eac15f295
Source noteuspto-grants-2011_05