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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424357Generated: October 29, 2026

Benzoic Acid → ON-013100

https://huagongshe.com/reaction/424357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic AcidHCID 243—
ReactantPiperidineHCID 8082—
Reactant2,4,6-TrimethoxybenzaldehydeHCID 70019—
ReactantHCID 11357417HCID 11357417—
SolventTolueneHCID 1140—
ProductON-013100HCID 1126941862.5%

Reaction Steps

A mixture of the 2-((3-hydroxy-4-methoxybenzyl)sulfonyl)acetic acid (1.9 g, 7.3 mmol, 1 eq), 2,4,6-trimethoxybenzaldehyde (1.58 g, 8.0 mmol, 1.1 eq.), benzoic acid (134 mg, 0.15 eq.) and piperidine (81 mg, 0.13 eq.) in toluene (50 mL) was heated at reflux temperature for 2-3 h with continuous removal of water using a Dean-Stark trap. When the reaction was complete by TLC analysis, the reaction mixture was cooled to room temperature. Water was added and the resulting mixture was extracted with ethyl acetate (3×50 mL). The combined organic extract was washed with saturated aqueous sodium bicarbonate solution (50 mL), dilute hydrochloric acid (50 mL), and water (50 mL) and dried (sodium sulfate). Volatile components were removed in vacuo to yield the crude product, which was purified by recrystallization from isopropanol to yield 1.8 g (62.5%) of the desired (E)-5-((2,4,6-trimethoxystyryl-sulfonyl)methyl)-2-methoxyphenol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106033B2
Source datasetuspto-grants-2012_01
ORD IDord-60944c59e79446039e45c3efd8ffe6c9
Source noteuspto-grants-2012_01