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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2396868Generated: October 30, 2026

Acetic Anhydride → HCID 18179293, compound

https://huagongshe.com/reaction/2396868

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantPerchloric AcidHCID 24247—
Reactant3-MethyltetrahydrofuranHCID 98230—
ProductHCID 18179293HCID 18179293154.9%

Reaction Conditions

Temperature70 °C

Reaction Steps

Into a 3,000-ml four-necked flask equipped with a stirrer, a thermometer, and a silica gel tube were introduced 1,200 g (16.64 mol) of tetrahydrofuran and 320 g (3.72 mol) of 3-methyltetrahydrofuran. The contents were cooled to 10° C. with an ice-cooled bath. Thereto was added 53 g of 70 wt % perchloric acid using a dropping funnel. Subsequently, 187 g of acetic anhydride was added thereto using another dropping funnel over a period of about 30 minutes so as not to cause heat generation. A reaction was then allowed to proceed for 8 hours while keeping the temperature of the mixture at 15° C. After completion of the reaction, 805 g of 20 wt % aqueous sodium hydroxide solution was added to terminate the reaction. The reaction vessel was then provided with a heater and a distiller, and was gradually heated to recover the unreacted monomers by distillation. Subsequently, 900 ml of n-butanol was added to the reaction mixture to dissolve the crude poly(tetramethylene glycol). The distiller was replaced with a reflux condenser to conduct a hydrolysis reaction at 90° C. for 5 hours. After completion of the reaction, the reaction mixture was cooled to about 70° C., and stirring was stopped to allow the reaction mixture to stand. The resulting alkaline aqueous layer as the lower layer was removed. To the remaining oil layer was added 500 g of distilled water. This mixture was stirred and washed with refluxing for 30 minutes and then allowed to stand, and the resulting aqueous layer as the lower layer was removed. This water-washing operation was repeated further three times. The finally obtained oil layer was transferred to a Claisen flask equipped with a distiller, and the n-butanol as solvent and the water present in a slight amount were removed to obtain 912 g of 3-methyltetrahydrofuran/tetrahydrofuran copolyether glycol, which was colorless and transparent. From its hydroxyl value determined by the acetylation method, H1NMR data, and DSC (Differential Scanning Calorimeter) data, this copolyether glycol was found to have a number-average molecular weight of 2,022, a 3-methyltetrahydrofuran unit/tetrahydrofuran ratio of 16/84 (by weight), and a melting point of 8° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05494990
Source datasetuspto-grants-1996_02
ORD IDord-7d616c96c6bf4f0fbdf1ea646f16f410
Source noteuspto-grants-1996_02