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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2392842Generated: October 25, 2026

p-Toluenesulfonic acid → Methyl 16-(2-tetrahydropyranyloxy)hexadecanoate

https://huagongshe.com/reaction/2392842

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 16-hydroxyhexadecanoateHCID 3496888—
SolventDichloromethaneHCID 6344—
ProductMethyl 16-(2-tetrahydropyranyloxy)hexadecanoateHCID 12687990—

Reaction Conditions

Temperature0 °C

Reaction Steps

100.26 g (0.35 mol) of methyl 16-hydroxyhexadecanoate, 0.60 g (3.5 mol) of p-toluenesulfonic acid and 350 ml of dichloromethane were introduced into a 1-l flask equipped with a stirrer and a dropping funnel and 32.39 g (0.385 mol) of dihydropyan was dropped thereto under stirring at 0° C. After the completion of the addition, the mixture was stirred at room temperature for additional 1 hour to thereby complete the reaction. Next, the reaction mixture was neutralized by adding 0.59 g (7 mmol) of NaHCO3 and filtered. After distilling off the solvent, crude methyl 16-(2-tetrahydropyranyloxy)hexadecanoate (III-a) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05801258
Source datasetuspto-grants-1998_09
ORD IDord-1fdc17b104f3439b9ca85abd0b80a480
Source noteuspto-grants-1998_09