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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 262394Generated: October 23, 2026

Hydrochloric Acid → 5-Chloromethylfurfural

https://huagongshe.com/en/reaction/262394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSucroseHCID 5988—
ReactantSodium dodecylbenzene sulphonateHCID 57371080—
CatalystHexadecyltrimethylammonium chlorideHCID 8154—
SolventTolueneHCID 1140—
Product5-ChloromethylfurfuralHCID 74191—

Reaction Steps

To a three-necked flask equipped with a condenser and a stirrer were added 5 g (0.014 mole) of a commercially available D-(+)-saccharose and two kinds of surface active agent, i.e., 47.1 mg (0.00014 mole) of cetyltrimethylammonium chloride and 51.3 mg (0.00014 mole) of sodium laurylbenzenesulfonate. Then, 5 ml of water and 30 ml of toluene were added thereto and the mixture was stirred. Thereafter, a molar excess of hydrogen chloride was passed through the mixture at room temperature for about 30 minutes with thorough stirring. After the reaction was continued at room temperature for a further 3 hours, the upper toluene layer was separated from the lower aqueous layer. Thirty milli-liters of toluene and the above two surface active agents of the same amounts as above were then freshly added to the aqueous layer. After the reaction was carried out at room temperature for 3 hours, the upper toluene layer was again separated. This toluene extraction operation was repeated three times in total. All the toluene layers were combined and filtered through Celite. The filtrate was neutralized with an aqueous sodium hydrogen carbonate solution, dried over anhydrous sodium sulfate and concentrated. Thus, about 2.6 g of 5 -chloromethylfurfural was obtained as a crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04154744
Source datasetuspto-grants-1979_05
ORD IDord-65db85bb71f34eae8caae5b5385e7a9a
Source noteuspto-grants-1979_05