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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650808Generated: October 31, 2026

1-Bromododecane → Benzeneacetic acid, 4-(dodecyloxy)-

https://huagongshe.com/reaction/1650808

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromododecaneHCID 8919—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 4-hydroxyphenylacetateHCID 28310—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductBenzeneacetic acid, 4-(dodecyloxy)-HCID 1033615263%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a dimethylformamide (DMF, 100 ml) solution of ethyl 4-hydroxyphenylacetate (18 g, 0.1 mol.) and dodecyl bromide (25 g, 0.1 mol.) was added potassium carbonate (15 g, 0.1 mol.). The mixture was stirred at 100° C. for one hour. To the reaction solution, after cooling, was added water (200 ml) and the mixture was subjected to extraction with isopropyl ether (IPE). The organic layer was washed with water, dried and concentrated under reduced pressure. The concentrate was dissolved in a mixture of methanol (100 ml) and tetrahydrofuran (THF, 100 ml). To the solution was added aqueous sodium hydroxide (10 g, 0.25 mol.), and the mixture was stirred at 50° C. The reaction solution was concentrated under reduced pressure, whose pH was adjusted to 4, followed by extraction with ethyl acetate. The organic layer was washed with water, dried and concentrated under reduced pressure to leave crude crystals. Recrystallization from hexane-IPE gave 4-dodecyloxyphenylacetic acid (1-e, 20 g, 63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04925868
Source datasetuspto-grants-1990_05
ORD IDord-16aebde31c074e54a8d11bff05acfb7c
Source noteuspto-grants-1990_05