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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2259607Generated: October 26, 2026

Dimethylformamide → 4-Chloro-2-[(2-methylene-3-butenyl)oxy]benzaldehyde

https://huagongshe.com/reaction/2259607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant1,3-Butadiene, 2-(bromomethyl)-HCID 90238—
Reactant4-Chloro-2-hydroxybenzaldehydeHCID 520101—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product4-Chloro-2-[(2-methylene-3-butenyl)oxy]benzaldehydeHCID 1900139284.6%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 4.1 g (0.026 mol) of 4-chloro-2-hydroxybenzaldehyde and 27 mL of DMF was added 5 g (0.034 mol) of 2-bromomethyl-1,3-butadiene and 7.2 g (0.052 mol) of potassium carbonate. The resulting mixture was heated at 70° C. for 4 h and then cooled to room temperature and poured into a mixture of 100 mL of water and 100 mL of methylene chloride. The aqueous layer was extracted with two 100 mL portions of methylene chloride and the combined organic layers were washed twice with 100 mL of water, twice with 100 mL of saturated sodium bicarbonate solution, dried over magnesium sulfate and concentrated to give 4.9 g of an oil. Purification by flash chromatography using 250 g of silica gel and eluting with 10:1 hexanes-EtOAc gave 2.6 g of the desired product. 200 MHz 1H NMR (CDCl3): δ4.82 (s, 2H), 5.18-5.42 (m, 4H), 6.45 (dd, 1H), 7.01 (s, 1H), 7.05 (d, 1H), 7.79 (d, 1H), 10.48 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05474998
Source datasetuspto-grants-1995_12
ORD IDord-f54ce4d81fe24c02a716a1fe9c707d60
Source noteuspto-grants-1995_12