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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2049014Generated: October 30, 2026

Diethyl Ether → 2,5-Diethoxybenzaldehyde

https://huagongshe.com/reaction/2049014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantMethane, dichloromethoxy-HCID 21004—
ReactantBenzene, 1,4-diethoxy-HCID 67150—
SolventDichloromethaneHCID 6344—
Product2,5-DiethoxybenzaldehydeHCID 343431493%

Reaction Steps

A mixture of 1,4-diethoxybenzene (24.9 g 0.150 mole) and 1,1-dichloromethyl methyl ether (18 g., 0.157 mole) in methylene chloride (80 ml.) was added with stirring during 20 minutes to a solution of stannic chloride (39 g., 0.150 mole) in methylene chloride (150 ml.) at approximately 0° C. The solution was then stirred at this temperature for 5 minutes and quenched by addition of aqueous hydrochloric acid (6 N., 100 ml.) which was added rapidly. The organic phase was separated washed with saturated aqueous sodium bicarbonate, dried over anhydrous magnesium sulfate, filtered, and the solvent removed from the filtrate by evaporation under reduced pressure to yield a crystalline solid (29 g.) m.p. 57°-59° C. Recrystallation (from ether) gave 2,5-Diethoxybenzaldehyde (27.1 g., 0.138 mole, 93%) m.p. 60°-61° I.R.: 1738 cm-1 (aldehyde CO).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04196127
Source datasetuspto-grants-1980_04
ORD IDord-d39a3c9629374433a3d4de7c8552e137
Source noteuspto-grants-1980_04