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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292157Generated: October 30, 2026

Diethyl Sulfate → HCID 14330446, compound

https://huagongshe.com/reaction/2292157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl SulfateHCID 6163—
ReactantHCID 14330445HCID 14330445—
ReactantPotassium tert-butoxideHCID 23665647—
SolventEthanolHCID 702—
ProductHCID 14330446HCID 14330446—

Reaction Steps

To a solution of ethyl 6-hydroxy-2-(ethoxycarbonylmethylthio)-phenylacetate (20.0 g) in anhydrous ethanol (200 mL) is added diethyl sulfate (10.3 g). To this is added in portions solid potassium t-butoxide (7.52 g), keeping the temperature below 30° with a cold-water bath. After stirring overnight at room temperature, the solvent is removed in vacuo and the residue is mixed with ether and water. The layers are separated and the organic layer is washed with ice-cold sodium hydroxide (0.5N, 40 mL) to remove starting material. The ether layer is washed with water to neutrality, dried over anhydrous magnesium sulfate, filtered and the filtrate is evaporated in vacuo to give (as shown by NMR) ethyl 6-ethoxy-2-(ethoxycarbonylmethylthio)-phenylacetate as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04801605
Source datasetuspto-grants-1989_01
ORD IDord-e147801ec47a4424b1d5b18c37318e29
Source noteuspto-grants-1989_01