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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328862Generated: October 25, 2026

Benzyl Chloride → (+/-)-6-Benzyloxy-2,5,7,8-tetramethylchroman-2-carboxylic acid

https://huagongshe.com/reaction/328862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
ReactantTroloxHCID 40634—
Reactant(+/-)-Benzyl 6-benzyloxy-2,5,7,8-tetramethylchroman-2-carboxylateHCID 21483865—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product(+/-)-6-Benzyloxy-2,5,7,8-tetramethylchroman-2-carboxylic acidHCID 9905948—

Reaction Steps

To a mixture of 0.5 g. of (±)-6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid and 1.3 g. of anhydrous potassium carbonate in 3 ml. of dimethylsulfoxide was added 1.0 g. of benzyl chloride. This mixture was stirred at 23° overnight to give a solution containing (±)-benzyl 6-benzyloxy-2,5,7,8-tetramethylchroman-2-carboxylate. To this solution was added 3 ml. of 1N sodium hydroxide solution and 2 ml. of dimethylsulfoxide and the resulting 2-phase solution was stirred at 100° for 16 hours. The mixture was cooled, diluted wth H2O, washed with ether, acidified with 2N HCl, and extracted with ether. The ether solutions were washed with brine, dried over sodium sulfate and stripped of solvent. The residue was crystallized from ether-30°-60° petroleum ether to give (±)-6-benzyloxy-2,5,7,8-tetramethylchroman-2-carboxylic acid as a white solid, m.p. 154.5°-155° .

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04018799
Source datasetuspto-grants-1977_04
ORD IDord-025cb78c4d4d49b18c388068d93d0874
Source noteuspto-grants-1977_04