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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433159Generated: November 1, 2026

Allyl bromide → N-(4-Acetyl-5-benzyloxy-2-bromo-phenyl)-N-allyl-acetamide

https://huagongshe.com/reaction/1433159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantLithium diisopropylamideHCID 2724682—
ReactantN-(4-Acetyl-5-benzyloxy-2-bromo-phenyl)-acetamideHCID 69059837—
SolventTetrahydrofuranHCID 8028—
ProductN-(4-Acetyl-5-benzyloxy-2-bromo-phenyl)-N-allyl-acetamideHCID 5793483358%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of N-(4-acetyl-5-benzyloxy-2-bromo-phenyl)-acetamide (1.03 g, 2.85 mmol) in anhydrous THF (20 ml) under nitrogen was cooled to −78° C. followed by the dropwise addition of LDA (2.1 ml, 2M solution, 4.3 mmol). The reaction was continued to stir for an hour at −78° C. and then quenched with allyl bromide (0.44 ml, 2.85 mmol). The reaction was allowed to warm to room temperature and continued to stir overnight. The solution was partitioned between EtOAc and water. The organics were collected and washed with water, brine and then dried (MgSO4). Purification by column chromatography in hexane/EtOAc (1:1) afforded a white solid (0.662 g, 58%). LC/MS: RT=2.703 min. 402/404 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612201B2
Source datasetuspto-grants-2009_11
ORD IDord-ac00bf304c034c559a71874a3180be30
Source noteuspto-grants-2009_11