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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38718Generated: October 25, 2026

Allyl bromide → 3-Chloro-4-(prop-2-en-1-yloxy)benzaldehyde

https://huagongshe.com/reaction/38718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant3-Chloro-4-hydroxybenzaldehydeHCID 17022—
ReactantSodium hydrideHCID 24758—
SolventWaterHCID 962—
Solventtetrahydrofuran N,N-dimethylformamideHCID 21974620—
Product3-Chloro-4-(prop-2-en-1-yloxy)benzaldehydeHCID 477003685.6%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of 3-chloro-4-hydroxybenzaldehyde (5.0 g, 31.9 mmol) in DMF/THF 1:3 (120 mL) is added NaH (1.67 g of a 55% dispersion in mineral oil, 38.3 mmol) in four portions. The mixture is stirred at rt for 1 h before allylbromide (9.66 g, 79.8 mmol) is added. The reaction mixture is heated to 65° C. for 18 h, diluted with water (250 mL) and extracted with diethyl ether (3×250 mL). The organic extracts are washed with water (250 mL), combined and concentrated. The remaining oil is chromatographed on silic gel with heptane/EA 4:1 to afford 4-allyloxy-3-chlorobenzaldehyde (5.37 g) as an almost colourless oil. LC: tR=0.95 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524752B2
Source datasetuspto-grants-2013_09
ORD IDord-482bcd3dcc48433ea236a8b74dc6f9fd
Source noteuspto-grants-2013_09