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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968926Generated: October 26, 2026

Sodium Acetate → 9-Methoxy-nonanal

https://huagongshe.com/reaction/1968926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AcetateHCID 517045—
ReactantCornforth reagentHCID 2724130—
Reactant9-Methoxy-1-nonanolHCID 12077348—
SolventDichloromethaneHCID 6344—
Product9-Methoxy-nonanalHCID 8585643154.4%

Reaction Steps

a 50-mL, one-necked, round-bottom flask equipped with a magnetic stirrer and stir bar was charged with 9-methoxy-nonanol (1.0 g, 5.9 mmol), dichloromethane (10 mL), molecular sieves (1.0 g, 3A), sodium acetate (0.1 g) at room temperature. The reaction mixture was stirred at room temperature under nitrogen for 5 minutes. The reaction mixture was charged with pyridinium dichromate (4.7 g, 12.5 mmol) and stirred overnight. The progress of reaction was monitored by TLC (Note 1). After completion of the reaction, the reaction mixture was filtered through a bed of silica gel (˜15 g). The filtrate was evaporated in vacuo to obtain a crude compound. This was purified by column chromatography using silica gel column (250-400 mesh, 40 g). A solvent gradient of ethyl acetate in hexane (10-50%) was used to elute the product from the column. All fractions containing the desired pure product were combined and concentrated in vacuo to give pure 9-methoxy-nonanal (lot D-1027-156, 553 mg, 54.4%). Completion of the reaction was monitored by thin layer chromatography (TLC) using a thin layer silica gel plate; eluent: 60% ethyl acetate in hexanes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426445B2
Source datasetuspto-grants-2013_04
ORD IDord-edb2da7ddc294bf6a64fd3a025292d3a
Source noteuspto-grants-2013_04