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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918228Generated: November 1, 2026

Tetrahydrofuran → HCID 86733703, compound

https://huagongshe.com/reaction/918228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 86733704HCID 86733704—
SolventEthanolHCID 702—
ProductHCID 86733703HCID 86733703—

Reaction Steps

3.6 grams of a random copolymer of N-vinylphthalimide/N-vinylcarbazole (9.2/90.8 mole percent) are dissolved in a solution containing 100 milliliters of tetrahydrofuran and 10 milliliters of ethanol. After the copolymer has been dissolved, 0.13 grams hydrazine hydrate (85%) were added and the solution thereafter heated to boiling under refluxing conditions overnight. At the end of this interval, the solution apparently remains unchanged, it retaining its characteristic yellow color. An additional 2.6 grams of hydrazine hydrate are then added and the solution refluxed for an additional two days. At the end of this time, the characteristic yellow color of the solution has disappeared and a white precipitate formed. The solution is now allowed to cool to room temperature and the precipitate removed by filtration. This precipitate is believed to be phthalhydrazide. The polymer is separated from the solution by precipitation with hexane in a Waring blender. The number average molecular weight of the polymeric product is about 78,000.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03970602
Source datasetuspto-grants-1976_07
ORD IDord-d3328977e96a4dbab0cbe1d504013b0f
Source noteuspto-grants-1976_07