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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2246244Generated: November 3, 2026

Allyl bromide → HCID 86617963, compound

https://huagongshe.com/reaction/2246244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantHCID 86617964HCID 86617964—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86617963HCID 86617963—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a stirred solution of the product from Step A (4.51 g, 14.2 mmol) in THF (150 mL) was added potassium hexamethyldisilazide (65.0 mL, 0.5M in toluene, 32.5.0 mmol) at −78° C. The resulting mixture was stirred at −78° C. for 30 min. Allyl bromide (6.2 mL, 71.7 mmol) was then added. After stirring at −78° C. for 2 h, the reaction was quenched with saturated aqueous ammonium chloride solution. The organic phase was separated and the aqueous phase was extracted with two portions of ethyl acetate. The combined organic layers were washed with brine and concentrated in vacuo. Purification by flash chromatography (30:70 hexanes/ethyl acetate) afforded the desired product (major diastereoisomer from the reaction).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687492B2
Source datasetuspto-grants-2010_03
ORD IDord-86952a3b88fd462f88a0994b070a711b
Source noteuspto-grants-2010_03