HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248860Generated: October 25, 2026
Vinyl isobutyl ether → 4-(p-Tert.-butylphenyl)-3-methyl-6-isobutoxy-5,6-dihydropyran
https://huagongshe.com/reaction/248860
Participants
| Role | Name | HCID | Charge |
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| Reactant | Vinyl isobutyl ether | HCID 7992 | — |
| Reactant | 2-Propenal, 3-[4-(1,1-dimethylethyl)phenyl]-2-methyl- | HCID 114659 | — |
| Catalyst | Hydroquinone | HCID 785 | — |
| Product | 4-(p-Tert.-butylphenyl)-3-methyl-6-isobutoxy-5,6-dihydropyran | HCID 70388635 | 30.7% |
Reaction Steps
3,000 g of 3-(4-tert.-butylphenyl)-2-methylprop-2-enal III and 2,000 g of vinyl isobutyl ether IV are introduced into a 10 l stirred autoclave, and 5 g of hydroquinone are added to the reaction mixture for stabilization. The autoclave is closed and then flushed with nitrogen, after which it is heated to 220° C., maintained under these conditions for 18 hours and then let down and opened. The reaction mixture (4,855 g) consists of about 39.6% of the desired product V. When the reaction mixture is worked up by fractionation in a laboratory column containing 10 sieve trays, a total of 1,379 g of the compound V of boiling point 135°-146° C. under 2 mbar are obtained from the 1,923 g shown to be present in the crude mixture by gas chromatographic analysis. This corresponds to a yield of 23%, based on the starting material III employed. 1,745 g of III, which contains some product V, are recovered. The last-mentioned amounts are reused for the reaction with vinyl isobutyl ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05212183 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-271966fa3bd34eb7b7b40b0f1c058e96 |
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| Source note | uspto-grants-1993_05 |
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