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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058542Generated: October 30, 2026

Hydrochloric Acid → HCID 15511212, compound

https://huagongshe.com/reaction/1058542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2,6-DimethoxyphenolHCID 7041—
ReactantPentan-3-yl methanesulfonateHCID 160750—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
ProductHCID 15511212HCID 15511212100.2%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a yellow solution of 38.5 g 2,6-dimethoxy phenol (0.25 mol) and 83.1 g methanesulfonic acid 1-ethyl-propyl ester (0.50 mol) in 500 ml dimethylsulfoxide was added under stirring at 50° C. a solution of 56,1 g potassium tert-butylate (0.50 mol) in 500 ml dimethylsulfoxide over 4 h. After additional 2.8 g potassium tert-butylate (0.025 mol) were added, stirring at 50° C. was continued for lh. The reaction mixture was distributed between 500 ml ethyl acetate and 600 ml 1N HCl. The organic layer was washed twice with 250 ml, a total of 500 ml deionized water and the aqueous layers were extracted sequentially with 250 ml ethyl acetate. The combined organic layers were dried over ca. 25 Na2SO4, filtered and the solvent was evaporated by rotary evaporation (50° C./≧1 mbar) affording 56.2 g (100.2%) of the title product as an orange oil, which was used without purification in the next step (bp. 90° C./0.03 mbar).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06518048B2
Source datasetuspto-grants-2003_02
ORD IDord-bcb95f537677498095fcf5b959762372
Source noteuspto-grants-2003_02