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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376309Generated: October 31, 2026

Pyridine → HCID 86751189, compound

https://huagongshe.com/reaction/1376309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant2-MethoxypropeneHCID 8300—
Reactant1,4-DioxaneHCID 31275—
ProductHCID 86751189HCID 86751189—

Reaction Steps

24.0 g of 2-methoxypropene are slowly added dropwise at 10° C. to a solution of 20.0 g of partially hydrogenated poly-4-hydroxystyrene (Maruka Lyncur PHM-C, content of cycloaliphatic structural units about 10 mol %), a catalytic quantity of 4-toluenesulfonic acid and a catalytic quantity of pyridine in 140 ml of 1,4-dioxane. The reaction mixture is stirred at room temperature for 24 h; the reaction solution is subsequently eluted slowly through a column into which 50.0 g of a strongly basic macroporous anion exchanger based on sytrene/divinylbenzene copolymer (Amberlyst® A-26) have been washed. The polymer is precipitated by introducing the reaction solution into a mixture of water and isopropanol, filtered off with suction, washed with a mixture of water and isopropanol and dried to constant weight. 24.0 g of poly[4-(1-methoxy-1-methylethoxy)styrene/4-(1-methoxy-1-methylethoxy)vinylcyclohexane/4-hydroxystyrene/4-vinylcyclohexanol] are obtained, in which according to thermogravimetric analysis (TGA) 65 mol % of the original OH groups have been protected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663038
Source datasetuspto-grants-1997_09
ORD IDord-cd7b4b0e09474bbfb5672f62329bcbf0
Source noteuspto-grants-1997_09