HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9701Generated: October 23, 2026
N-methyl-2-pyrrolidone → [4-(Ethenyloxy)phenyl](phenyl)methanone
https://huagongshe.com/en/reaction/9701
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | 4-Hydroxybenzophenone | HCID 14347 | — |
| Catalyst | Zinc naphthenate | HCID 13879901 | — |
| Product | [4-(Ethenyloxy)phenyl](phenyl)methanone | HCID 21987723 | — |
Reaction Steps
A mixture of 650 g of 4-hydroxybenzophenone (98% by weight, Avocado, Research Chemicals Ltd.), 750 ml of N-methylpyrrolidone (>99% by weight, BASF AG) and 60 g of zinc naphthenate (Nusa; zinc salts of naphthenic acids, zinc content 12% by weight) was charged with stirring to a 2.5 l autoclave and flushed with nitrogen. After it had been heated to 190° C., injection was carried out first with nitrogen to 2 bar and then with acetylene to 20 bar. During the reaction, further acetylene was supplied to replace that consumed by reaction, so as to maintain a constant pressure of 20 bar. After a reaction time of 12 hours the batch was cooled to 20–25° C. (room temperature) and let down to atmospheric pressure. The solvent was distilled off under reduced pressure at a bridge temperature of from 70 to 80° C. with a pressure of 1 mbar (absolute). 310 g of Pluriol® E 600 (polyethylene glycol, trademark of BASF AG) were then added and the product was purified by a Sambay distillation at 1.2 mbar (absolute) and a bridge temperature of 163° C. This gave a total of 522 g of 4-vinyloxybenzophenone having a purity of from 96 to 99% by weight and a melting point of 58° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07091296B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-63c05866145e472c88a3d838aafd9c42 |
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| Source note | uspto-grants-2006_08 |
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