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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 864309Generated: November 1, 2026

Allyl bromide → HCID 178458129, compound

https://huagongshe.com/reaction/864309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
ReactantHCID 19958191HCID 19958191—
ProductHCID 178458129HCID 17845812989%

Reaction Conditions

Temperature0 °C

Reaction Steps

Diethyl 1-hydroxypyrrolo[3,2-b]pyridine-5,6-dicarboxylate (6.2 g, 0.022 mol)is dissolved in (200 mL) dry tetrahydrofuran and cooled to 0° C. under nitrogen. Sodium hydride (0.77 g, 0.033 mol) is added in portions over ten minutes and the reaction is stirred for 30 minutes at 0° C. Allyl bromide (2.01 mL, 0.024 mol) is added all at once to the suspension and the mixture allowed to warm to room temperature and then stirred for 16 hours. The mixture is filtered and the filtrate concentrated in vacuo. The resulting oil is chromatographed using 4:1 hexanes/ethyl acetate and then increasing the polarity to 2:1 hexanes/ethyl acetate to give the product as a yellow oil in 89% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05563113
Source datasetuspto-grants-1996_10
ORD IDord-7a0ac548835147f79c330c4f4c15bb9e
Source noteuspto-grants-1996_10