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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485183Generated: October 25, 2026

Water → Ethyl 4-(2-formyl-3-hydroxyphenoxymethyl)benzoate

https://huagongshe.com/reaction/485183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl 4-(bromomethyl)benzoateHCID 954261—
ReactantAR-260HCID 15312034—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
ProductEthyl 4-(2-formyl-3-hydroxyphenoxymethyl)benzoateHCID 9861133—

Reaction Steps

To a stirred solution of 2-hydroxy-6-methoxymethoxybenzaldehyde (0.91 g, 5.1 mM) in dry dimethyl sulphoxide (8 ml) was added potassium t-butoxide (0.57 g, 5.1 mM) with exclusion of moisture. After 10 mins, ethyl 4-bromomethylbenzoate (1.22 g, 5 mM) was added and the whole stirred at room temperature (18 hrs). The reaction mixture was poured into water (100 ml) and the liberated oil extracted into ether. The combined extracts were washed with 5% sodium carbonate solution, water, dried (sodium sulphate) and evaporated. The residual oil (ethyl 4-(2-formyl-3-methoxymethoxyphenoxymethyl)benzoate was dissolved in ethanol (30 ml) and treated with 3 M hydrochloric acid (30 ml) with stirring at 60° C. (30 mins). The solid was filtered off, washed with water, dried, and recrystallised from ethanol/water to give ethyl 4-(2-formyl-3-hydroxyphenoxymethyl)benzoate, m.p. 105°-ω° C. (identical to a sample previously prepared, Example 5(B)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04535183
Source datasetuspto-grants-1985_08
ORD IDord-052949e770eb41f985c1ab10e72457d6
Source noteuspto-grants-1985_08