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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1758119Generated: November 2, 2026

Sulfuric Acid → CID 3084433

https://huagongshe.com/reaction/1758119

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium TetrafluoroborateHCID 4343483—
SolventWaterHCID 962—
ProductCID 3084433HCID 3084433—

Reaction Conditions

Temperature30 °C

Reaction Steps

In the same reaction apparatus as in Example 15, 126 g of 25% fuming sulfuric acid containing 0.9 g of sodium borofluoride was dropped from the dropping funnel into 600 g of tetrahydrofuran at -10° C. with stirring over 40 minutes, after which the resulting mixture was subjected to reaction at -10° C. for one hour. The conversion at the end of this reaction was 39%. Then, the reaction mixture was heated to 30° C. and subjected to reaction at this temperature for 2 hours, after which 10 g of water was added to the mixture to terminate the polymerization. The final conversion was 60%. Then, 530 g of water was added (sulfuric acid concentration was about 20%), and the reaction solution was heated and hydrolyzed in an oil bath at 80° C. while distilling off the unreacted tetrahydrofuran in the same manner as in Example 1, and then 204 g of a 48% by weight sodium hydroxide solution (corresponding to 90% neutralization degree) was added continuously over a period of one hour while the internal temperature was kept at 100° C. to continue the hydrolysis. The recovery of unreacted tetrahydrofuran by distillation was continued during these operations. Then, in the same manner as in Example 1, the reaction mixture was allowed to stand to cause separation of layers, after which the aqueous layer was withdrawn. The PTMG layer was washed at 80° C. for one hour with 350 g of a 20% by weight aqueous sodium sulfate solution. After separating and withdrawing the aqueous layer again, the volatile matters were removed in the same manner as in the foregoing Examples and the residue was filtered through a 10-μ mesh membrane filter to obtain PTMG. The results of the analyses of the thus obtained PTMG were as shown in Table 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04371713
Source datasetuspto-grants-1983_02
ORD IDord-6999d49250824c6db4d91ac516e42cb1
Source noteuspto-grants-1983_02