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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980324Generated: October 30, 2026

Trimethylhydroquinone → HCID 13633545, compound

https://huagongshe.com/reaction/980324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylhydroquinoneHCID 12785—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 54100633HCID 54100633—
CatalystZincchlorideHCID 3007855—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 13633545HCID 1363354543.5%

Reaction Steps

Molten zinc chloride (0.22 g), trimethylhydroquinone (2.47 g) and anhydrous dioxane (10 cc) are introduced into a 250 cc reactor. The mixture is heated to 40°-45° C. and a solution of 1,7,11,15-tetrachloro-3,7,11,15-tetramethyl-hexadec-2-ene (6.8 g) in dioxane (7 cc) is then added over the course of 20 minutes. Stirring is continued for 1 hour 30 minutes. The reaction mixture is poured into an aqueous solution (50 cc) of ammonium chloride (100 g/liter). The batch is extracted with ethyl acetate (twice 50 cc) and the organic phases are then dried over magnesium sulphate. After filtration and evaporation of the solvent, 2,5,7,8-tetramethyl-2-(4',8',12'-trichloro-4',8',12'-trimethyltridecyl)-chroman-6-ol is obtained in a yield of 43.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04636570
Source datasetuspto-grants-1987_01
ORD IDord-ad3faf10d9f84f2cbb43820e8583d231
Source noteuspto-grants-1987_01