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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344797Generated: November 1, 2026

Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) → 1-(4-Hydroxyphenyl)ethyl butyrate

https://huagongshe.com/reaction/344797

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
Reactant1-(4-(Tetrahydro-2-pyranyloxy)phenyl)ethyl butyrateHCID 54170443—
SolventMethanolHCID 887—
Product1-(4-Hydroxyphenyl)ethyl butyrateHCID 5413391113%

Reaction Steps

In 150 ml of methanol was dissolved 0.1 mole of the S-form of 1-(4-(tetrahydro-2-pyranyloxy)phenyl)ethyl butyrate, 1.1 g of pyridinium p-toluenesulfonate was added thereto, and the mixture was subjected to reaction at room temperature for 2 hours. Then, methanol was distilled under reduced pressure, to which 200 ml of ether was added, and the mixture was washed with water. The resulting ether layer was dried with anhydrous magnesium sulfate, and ether was distilled under reduced pressure to give S-form of 1-(4-hydroxyphenyl)ethyl butyrate (yield: 13%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05053507
Source datasetuspto-grants-1991_10
ORD IDord-f335a3f28ccc4b94847390381846f88d
Source noteuspto-grants-1991_10