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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1985061Generated: November 2, 2026

Allyl bromide → 1-[(Allyloxy)methyl]-2-iodobenzene

https://huagongshe.com/reaction/1985061

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium hydrideHCID 24758—
Reactant2-Iodobenzylic alcoholHCID 107629—
SolventTetrahydrofuranHCID 8028—
Product1-[(Allyloxy)methyl]-2-iodobenzeneHCID 11482716105.7%

Reaction Steps

To a THF (200 ml) solution of 2-iodo-benzyl alcohol (25 g, 107 mmol), at r.t., was added the NaH (5.12 g, 128 mmol) in small portions. After complete addition of the NaH the allyl bromide (11.1 ml , 128 mmol) was added via syringe. The mixture was stirred overnight at room temperature. The resulting white heterogeneous mixture was quenched with H20 (100 ml) and diluted with 300 ml of Et2O followed by washing with H2O (2×100 ml) and brine (1×100 ml). The organic layer was dried over MgSO4 and concentrated in vacuo to yield 31 g of 1-[(allyloxy)methyl]-2-iodobenzene as a faint yellow oil. HRMS (ESI+) calcd for C10H11IO m/z 273.9857 (M+H)+. Found 273.9855.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544717B2
Source datasetuspto-grants-2009_06
ORD IDord-084404e0005949d687e8e2d59509e101
Source noteuspto-grants-2009_06