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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181670Generated: October 27, 2026

Allyl bromide → Methyl 3-(allyloxy)-4-iodobenzoate

https://huagongshe.com/reaction/2181670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 3-hydroxy-4-iodobenzoateHCID 10378812—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductMethyl 3-(allyloxy)-4-iodobenzoateHCID 22481791100%

Reaction Steps

Methyl 3-hydroxy-4-iodobenzoate (2.0 g, 7.2 mmol) is dissolved in DMF (25 ml) in a dry flask under nitrogen. Allyl bromide (0.65 ml, 7.55 mmol) is added drop-wise, followed by the careful addition of 60% NaH (303 mg, 7.55 mmol). The reaction is stirred overnight at RT and then is diluted with H2O (30 ml). The mixture is extracted with EtOAc (3×30 ml), and the combined organics are washed with 50% saturated NaCl (4×25 ml), dried (MgSO4), filtered, and concentrated under high vacuum to an oil that solidified upon standing. The volatiles are removed in vacuo to obtain 2.28 g (100%) of methyl 3-(allyloxy)-4-iodobenzoate as a tan solid. HRMS (FAB) calcd for C11H11IO3+H: 318.9833, found 318.9831 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06894042B2
Source datasetuspto-grants-2005_05
ORD IDord-edb337a036a346a5a921d895a5f030d8
Source noteuspto-grants-2005_05