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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1991512Generated: October 31, 2026

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

https://huagongshe.com/reaction/1991512

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 H2O (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 numberUS07645780B2
Source datasetuspto-grants-2010_01
ORD IDord-61e5622b7f0546b2bfdd2e99d6041419
Source noteuspto-grants-2010_01