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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181673Generated: October 31, 2026

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

https://huagongshe.com/reaction/2181673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 4-hydroxy-3-iodobenzoateHCID 11346465—
SolventDimethylformamideHCID 6228—
ProductMethyl 4-(allyloxy)-3-iodobenzoateHCID 1118619660%

Reaction Steps

Methyl 4-hydroxy-3-iodobenzoate (1.85 g, 6.65 mmol) is dissolved in anhydrous DMF (15 mL) in a dry flask under nitrogen, treated with NaH (60% dispersion in oil, 265 mg, 6.65 mmol) and stirred for 1 h at RT. Allyl bromide (633 μL, 7.32 mmol) is added and the mixture is stirred for 16 h. The mixture is concentrated and the residue is partitioned between EtOAc (25 mL) and H2O (25 mL). The organic layer is washed with a 50% saturated mixture of 1:1 NaC/NaHCO3 (2×10 mL), dried (MgSO4) and concentrated to a yellow oil which solidified to a white solid upon standing (2.12 g). The crude material is chromatographed over 100 g slurry-packed silica gel, eluting with 10% EtOAc/hexane. The appropriate fractions are combined and concentrated to afford 1.27 g (60%) of methyl 4-(allyloxy)-3-iodobenzoate as a colorless oil which solidified on standing. MS for C11H11IO3 (EI) m/z: 318 (M)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06894042B2
Source datasetuspto-grants-2005_05
ORD IDord-5874123d145b41b18ad163ef88ad1818
Source noteuspto-grants-2005_05