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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356930Generated: October 26, 2026

3-Cyclopent-2-enyloxy-4-methoxybenzaldehyde → 3-Cyclopent-2-enyloxy-4-methoxybenzoic acid

https://huagongshe.com/reaction/356930

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Cyclopent-2-enyloxy-4-methoxybenzaldehydeHCID 22145828—
ReactantSodium ChloriteHCID 23668197—
ReactantMonosodium phosphateHCID 23672064—
Solventtert-ButanolHCID 6386—
Solvent2-Methyl-2-buteneHCID 10553—
Product3-Cyclopent-2-enyloxy-4-methoxybenzoic acidHCID 2214568971.3%

Reaction Steps

A solution of 3-cyclopent-2-enyloxy-4-methoxybenzaldehyde (7.70 g) in t-butanol (160 mL) and 2-methyl-2-butene (40 mL) is treated dropwise with an aqueous solution (150 mL) containing sodium chlorite (80% technical grade; 4.39 g) and sodium dihydrogen phosphate (38.49 g), and left to stand overnight. The resulting mixture is extracted with dichloromethane (2×250 mL), and the combined organic layers are dried over sodium sulfate, the solvent is removed under reduced pressure, and the resulting residue is recrystallized from ethyl acetate, to give 3-cyclopent-2-enyloxy-4-methoxybenzoic acid (5.89 g), in the form of a colorless solid. m.p. 160°-163° C. [Elemental analysis: C,66.4; H,6.0%; calculated: C,66.7; H,6.0%].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840724
Source datasetuspto-grants-1998_11
ORD IDord-3e441b73de6a4aa6a6057c9172883fda
Source noteuspto-grants-1998_11