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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752018Generated: October 27, 2026

Dimethoxymethane → HCID 67254607, compound

https://huagongshe.com/reaction/1752018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethoxymethaneHCID 8020—
ReactantLithium BromideHCID 82050—
ReactantSodium BicarbonateHCID 516892—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 67256194HCID 67256194—
SolventDiethyl EtherHCID 3283—
SolventChloroformHCID 6212—
ProductHCID 67254607HCID 67254607—

Reaction Steps

1-(4-Chlorobenzyl)-3,3-bis-hydroxymethyl-2-oxo-cyclopentancarboxylic acid methyl ester (Compound (XXVI), R2=CH3, Ym=4-Cl) (3.6871 g, 10.0 mmol) was dissolved in chloroform (14.5 ml), combined with dimethoxymethane (14.5 ml), lithium bromide (173.6 mg, 2.00 mmol) and p-toluenesulfonic acid monohydrate (190.2 mg, 1.00 mmol) and stirring was conducted at room temperature for 2 hours. After completion of the reaction, an aqueous solution of sodium hydrogen carbonate and diethyl ether were added, and the organic layer was separated. This was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was distilled away, and the residue was subjected to silica gel column chromatography (eluent; hexane:ethyl acetate=2:1 to 1:1) for purification to obtain the desired substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09162966B2
Source datasetuspto-grants-2015_10
ORD IDord-3dd5e35ae9a34c9d977c8e734995d97e
Source noteuspto-grants-2015_10