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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720846Generated: November 2, 2026

Methanol → HCID 1898172, compound

https://huagongshe.com/reaction/1720846

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
Reactant3,5-Di-tert-butyl-4-hydroxybenzene-1-sulfonyl chlorideHCID 15332942—
ProductHCID 1898172HCID 189817278.7%

Reaction Steps

To a mixture of 10.0 g (32.4 mmol) of 3,5-di-tertiary-butyl-4-hydroxybenzenesulfonyl chloride, prepared as described above, and 50 ml of anhydrous methanol was added 2.56 g (32.4 mmol) of pyridine. An exothermic reaction ensued resulting in a solution. The solution was stirred at room temperature for 30 minutes and poured into water. A white solid precipitate formed which was collected and dissolved in methylene chloride. The solution was washed with water, dried over magnesium sulfate and concentrated. The solid residue was recrystallized from heptane to give 7.66 g of, as a white crystalline product, methyl 3,5-di-tertiary-butyl-4-hydroxybenzenesulfonate (78.7% of theory); mp=116.5°-18° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05508140
Source datasetuspto-grants-1996_04
ORD IDord-efad250cd4114b6a80f044a2f5a8025f
Source noteuspto-grants-1996_04