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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850415Generated: October 30, 2026

Pyridine → HCID 19363503, compound

https://huagongshe.com/reaction/850415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethyl iodideHCID 6328—
ReactantSemicarbazide hydrochlorideHCID 11236—
ReactantHCID 19363318HCID 19363318—
ReactantPotassium tert-butoxideHCID 23665647—
SolventBenzeneHCID 241—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
ProductHCID 19363503HCID 1936350379%

Reaction Conditions

Temperature-5 °C

Reaction Steps

2-(2-Methoxy-5-methylphenyl)octanal (63.8 g, 0.257 mol), methyl iodide (160 ml, 2.57 mol) and benzene (300 ml) were mixed, and this solution was cooled to -5° C. Potassium t-butoxide (31.3 g, 0.279 mol) was added in such a manner that the temperature of the reaction mixture does not exceed 0° C., and the mixture was stirred at -2° C. for 0.5 hour. The reaction mixture was poured into ice water (200 ml) to stop the reaction. The aqueous layer was erected twice with ether (150 ml), and the organic layers were combined, washed with saturated brine (100 ml) and dried over anhydrous magnesium sulfate. The drying agent was filtered off, and the filtrate was concentrated under reduced pressure. Methanol (400 ml), an aqueous solution (110 ml) of semicarbazide hydrochloride (28.6 g, 0.257 mol) and pyridine (20.4 ml, 0.257 mol) were added to the obtained residue, and the mixture was stirred at room temperature for 0.75 hour. The precipitated crystals were collected by filtration, and washed with hexane. The crystals were dried to give 2-(2-methoxy-5-methylphenyl)octanal semicarbazide (64.7 g, 79%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06017919
Source datasetuspto-grants-2000_01
ORD IDord-a41ed2f97781426dab26fc76113ded29
Source noteuspto-grants-2000_01