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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1501284Generated: November 3, 2026

Cetyl Alcohol → HCID 117676213, compound

https://huagongshe.com/reaction/1501284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCetyl AlcoholHCID 2682—
ReactantHexaneHCID 8058—
ReactantTroloxHCID 40634—
Reactant2-Chloro-1-methylpyridinium iodideHCID 167069—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 117676213HCID 11767621365.4%

Reaction Steps

Under electromagnetic stirring, to a 100 mL reaction flask hexadecanol (970 mg, 4 mmol), 4-dimethylaminopyridine (1466 mg, 12 mmo), 2-chloro-1-methylpyridinium iodide (1533 mg, 6 mmol) and dioxane (20 mL) were added, and then to the reaction solution a solution of (±)-6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid (1001 mg, 4 mmol) in dioxane (20 mL) was slowly dropwise added. The reaction mixture was reacted for 12 h at room temperature under the protection of nitrogen gas and electromagnetic stirring. The solvent (dioxane) was removed by a rotary evaporator, and thereto diethyl ether (50 mL) was added. The resulting mixture was stirred for 2 h, and the precipitate was removed by filtration. The filtrate was concentrated to 10 mL, and isolated by column chromatography (the stationary phase was 230-400 mesh silica gel, the eluent was hexane:ethyl acetate=10:1), to obtain (±)-6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid hexadecyl ester (1242 mg, yield 65.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206192B2
Source datasetuspto-grants-2015_12
ORD IDord-6be803af474a4fc38cc030b8afc81754
Source noteuspto-grants-2015_12