HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918228Generated: November 1, 2026
Tetrahydrofuran → HCID 86733703, compound
https://huagongshe.com/reaction/918228
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 86733704 | HCID 86733704 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86733703 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03970602 |
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| Source dataset | uspto-grants-1976_07 |
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| ORD ID | ord-d3328977e96a4dbab0cbe1d504013b0f |
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| Source note | uspto-grants-1976_07 |
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