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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460099Generated: October 29, 2026

Sodium Thiosulfate Pentahydrate → Methyl 4-formyl-5-methylfuran-2-carboxylate

https://huagongshe.com/reaction/460099

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium Thiosulfate PentahydrateHCID 61475—
ReactantTriacetoxyperiodinaneHCID 159087—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 4-(hydroxymethyl)-5-methylfuran-2-carboxylateHCID 58824163—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductMethyl 4-formyl-5-methylfuran-2-carboxylateHCID 1550395870.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

Acetic acid 1,1-diacetoxy-3-oxo-1λ5-ioda-2-oxa-indan-1-yl ester (Dess-Martin reagent) (549 mg, 1.293 mmoles) in dry dichloromethane was added to a solution of 4-hydroxymethyl-5-methyl-furan-2-carboxylic acid methyl ester (16) (200 mg, 1.176 mmoles) in dry dichloromethane (9 ml) with cooling to 0° C. under an argon atmosphere. After stirring for 20 minutes, the mixture was diluted with diethyl ether (40 ml) and was poured into saturated aqueous sodium bicarbonate (30 ml) containing sodium thiosulphate pentahydrate (4 g) and agitated vigorously for 5 minutes. The organic phase was washed with saturated aqueous sodium bicarbonate (40 ml), water (50 ml) and brine (50 ml) and dried. After removal of the solvent, the residue was purified by flash chromatography, using petrol/diethyl ether 4:1 v/v as eluent, to afford compound 157(140 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196089B2
Source datasetuspto-grants-2007_03
ORD IDord-a7ea4afc99d04686911f50a55bc7c37d
Source noteuspto-grants-2007_03