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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271208Generated: November 1, 2026

Sodium Bicarbonate → HCID 18407199, compound

https://huagongshe.com/reaction/2271208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantN-acetyl-N-[2-(1,3-dioxolan-2-yl)benzyl]-2-phenoxyanilineHCID 18407221—
SolventAcetoneHCID 180—
ProductHCID 18407199HCID 1840719985.1%

Reaction Steps

In 40 ml of acetone was dissolved 2.81 g of N-acetyl-N-[2-(1,3-dioxolan-2-yl)benzyl]-2-phenoxyaniline synthesized in the same manner as in Example 3, and then 0.10 g of p-toluenesulfonic acid monohydrate was added, followed by stirring at room temperature for 6 hours. To the reaction solution was added a saturated aqueous sodium bicarbonate solution, the acetone was concentrated under reduced pressure, and the residue was extracted with ethyl acetate, washed with a saturated aqueous sodium bicarbonate solution and a saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate. After removal of the drying agent by filtration, the solvent was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent; ethyl acetate-hexane=1:3), dried and allowed to stand at room temperature to give 2.12 g of N-acetyl-N-(2-formylbenzyl)-2-phenoxyaniline as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06333358B1
Source datasetuspto-grants-2001_12
ORD IDord-91fff61f1ce140ee804e6a0aff341141
Source noteuspto-grants-2001_12