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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063828Generated: November 3, 2026

3-Methoxyphenol → HCID 10060488, compound

https://huagongshe.com/reaction/1063828

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethoxyphenolHCID 9007—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
SolventDiethyl EtherHCID 3283—
Solvent3,4-dihydro-2H-pyranHCID 8080—
ProductHCID 10060488HCID 1006048824,786.6%

Reaction Steps

A solution of 22 gm (177.4 mMol) 3-methoxyphenol in 30 mL dihydropyran was added dropwise to a solution of 100 mg (0.525 mmol) p-toluenesulfonic acid monohydrate in 10 mL dihydropyran while cooling in an ice/water bath. After stirring for 1 hour the reaction mixture was diluted with 300 mL diethyl ether and then washed sequentially with 100 mL 0.1 N sodium hydroxide and 100 mL saturated aqueous sodium chloride. The remaining organic phase was dried over magnesium sulfate and concentrated under reduced pressure. The resulting oil was distilled. The fraction distilling at 110–130° C. was collected and then partitioned between 5 N sodium hydroxide and diethyl ether. The organic phase was separated, washed sequentially with water and saturated aqueous sodium chloride, dried over magnesium sulfate and concentrated under reduced pressure to provide 27.1 gm (73%) of tetrahydropyran-2-yl 3-methoxyphenyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06967201B1
Source datasetuspto-grants-2005_11
ORD IDord-82a9d0b28638495f904dab2427989a8e
Source noteuspto-grants-2005_11