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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2294518Generated: October 29, 2026

Diethyl Ether → HCID 11056735, compound

https://huagongshe.com/reaction/2294518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 86751624HCID 86751624—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11056735HCID 1105673582.1%

Reaction Steps

20 ml of 2.5N sodium hydroxide are added to 240 mg (0.51 mmol) of n-decyl n-decyl β-D-galactofuranoside uronate solubilized in 5 ml of THF and the mixture is allowed to stand at room temperature for 3 hours. 30 ml of ethyl ether are added and then after decanting, the aqueous phase is washed with 30 ml of ethyl ether. The aqueous phase is acidified with 50% HCl at 0° C. to pH=2 and then extracted three times with 30 ml of ethyl acetate. The organic phases are pooled, washed with 30 ml of water, dried over magnesium sulphate (2 g) and evaporated. 140 mg of n-decyl β-D-galactofuranoside uronic acid are then obtained (82% yield) in the form of a gum. *Rf=0.67 (dichloromethane/methanol-1/1-v/v) *13C NMR in CD3OD

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05688929
Source datasetuspto-grants-1997_11
ORD IDord-83dda2718db14f3bbadb20813a876140
Source noteuspto-grants-1997_11