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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956592Generated: November 1, 2026

Water → 2-chloro-6-phenoxybenzaldehyde

https://huagongshe.com/reaction/1956592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPhenolHCID 996—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-6-fluorobenzaldehydeHCID 67847—
SolventDimethylacetamideHCID 31374—
Product2-chloro-6-phenoxybenzaldehydeHCID 1866360283.6%

Reaction Steps

A mixture of 15.8 g (100 mmol) of 2-chloro-6-fluorobenzaldehyde, 9.4 g (100 mmol) of phenol and 20.7 g (150 mmol) of potassium carbonate in 150 ml of dimethylacetamide is heated under reflux for 4 hours. The mixture is allowed to cool, water is added and the mixture is extracted 3× with tert-butyl methyl ether. The organic phases are washed with 2N sodium hydroxide solution and brine, dried over sodium sulfate and concentrated. Bulb tube distillation (175° C., 0.04 mbar) yields 19.46 g (83.64 mmol)=83.6% of 2-chloro-6-phenoxy-benzaldehyde in the form of a yellow oil; 1H-NMR (CDCl3, 200 MHz): 6.75-7.45 (m, 8H); 10.58 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05780501
Source datasetuspto-grants-1998_07
ORD IDord-6147f8466c2540c6a618d7bf44609f38
Source noteuspto-grants-1998_07