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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272277Generated: October 30, 2026

Allyl Alcohol → 1-Allyloxy-3-bromo-5-fluorobenzene

https://huagongshe.com/reaction/272277

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl AlcoholHCID 7858—
ReactantSodium hydrideHCID 24758—
Reactant1-Bromo-3,5-difluorobenzeneHCID 136313—
SolventDimethylacetamideHCID 31374—
Product1-Allyloxy-3-bromo-5-fluorobenzeneHCID 2204657069.1%

Reaction Steps

To a DMA (400 ml) solution of allyl alcohol (8.9 g, 0.154 mol), at room temperature (r.t.) is added NaH (60% oil dispersion) (6.4 g, 0.160 mol) in portions. The mixture is stirred at r.t. for 1.5 h followed by the slow addition of 3,5-difluoro bromobenzene (17.9 ml, 30 g, 0.155 mol). The reaction mixture is stirred at r.t. overnight. The reaction is quenched by the addition of 1500 ml of water and extracted with ether (4×300 ml). The organic layer is dried over MgSO4 and concentrated at reduced pressure to yield 24.6 g (69%) of a colorless oil after flash chromatography (pentane, rf.=0.3). Anal. Calc. for C9H8BrFO: C, 46.78; H, 3.49. Found: C. 46.18, H, 3.45. Calculated mass for C9H8OFBr: 229.97. Mass found for C9H8OFBr: (OAMS) ES−: 189.0 (M-allyl)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456163B2
Source datasetuspto-grants-2008_11
ORD IDord-82403a9db12147acad1c4360621efead
Source noteuspto-grants-2008_11