HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192763Generated: November 1, 2026
1,2-Dichloroethane → HCID 86640907, compound
https://huagongshe.com/reaction/2192763
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | HCID 97793 | HCID 97793 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86640907 | HCID 86640907 | 82.5% |
Reaction Steps
The 5-norbornene-2-carboxylic acid/ethylene copolymer (13.2 g, 79.64 mmol) that was polymerized in (2), 4′-hydroxy-4-methoxy chalcone (Aldrich, 18.4 g, 72.4 mmol), EDC (Aldrich, 22.2 g, 115.84 mmol), and HOBT (Aldrich, 14.7 g, 108.6 mmol) were put into the 2-neck flask having the volume of 250 ml, and then dissolved in 100 ml of DMF. After the temperature was reduced to 0° C., triethylamine (Aldrich, 50 ml, 362 mmol) was slowly dropped on the reaction solution. After the temperature was increased to normal temperature and maintained for 3 hours, when the reaction was finished, the reaction solution was dropped on a large amount of methanol to precipitate the polymer, and the polymer was filtered to obtain the 5-norbornene-2-(4′-hydroxy-4-methoxy chalcone)ester/ethylene copolymer to which the 1-(3-methoxy phenyl)-3-(2-hydroxyphenyl)-2-propenone functional group was introduced (yield: 82.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08329841B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-6427f75520b241a88623d5f4c71b7fb1 |
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| Source note | uspto-grants-2012_12 |
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