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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415186Generated: October 31, 2026

Hydrochloric Acid → 4-[2-(4,4-Dimethyl-chroman-7-yl)-heptyloxy]-benzoic acid

https://huagongshe.com/reaction/2415186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantPotassium HydroxideHCID 14797—
Reactant4-[2-(4,4-Dimethyl-chroman-7-yl)-heptyloxy]-benzoic acid methyl esterHCID 12149067—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product4-[2-(4,4-Dimethyl-chroman-7-yl)-heptyloxy]-benzoic acidHCID 1017889279.4%

Reaction Conditions

Temperature45 °C

Reaction Steps

A solution of 4-[2-(4,4-dimethyl-chroman-7-yl)-heptyloxy]-benzoic acid methyl ester (0.474 g, 1.15 mmole) in 8 mL of ethanol was treated with a solution of potassium hydroxide (1.3 g) in 5 mL of water. THF (4 mL) was added and the mixture was heated at 45° C. for two hours, diluted with 20 mL of water and the pH was adjusted to 2 with concentrated HCl. The mixture was then extracted with three 20 mL portions of ethyl acetate. The combined organic extracts were dried over MgSO4, filtered and concentrated in vacuo to give a pale yellow foam. The product was purified by recrystallization from acetonitrile/water to yield 0.362 g of 4-[2-(4,4-dimethyl-chroman-7-yl)-heptyloxy]-benzoic acid (1) as a white solid. M.p.: 91.5-93.3° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06818652B2
Source datasetuspto-grants-2004_11
ORD IDord-d3f9ebadae2a474789021ad2ce4d1fb1
Source noteuspto-grants-2004_11