HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885771Generated: October 30, 2026
Acetaldehyde → 2,2,6-Trimethyl-5-isopropenyltetrahydropyran
https://huagongshe.com/reaction/885771
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | 5-Hepten-2-ol, 2,6-dimethyl- | HCID 80183 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2,2,6-Trimethyl-5-isopropenyltetrahydropyran | HCID 66733857 | 55.9% |
Reaction Steps
42 g of acetaldehyde in 600 ml diethylether were placed in a 2 liter three-necked flask and cooled to 0° C. 140 g of a 48% solution of boron trifluoride diethyl etherate were then added and stirred for 10 minutes at 0° C. 124 g of 2,6-dimethyl-hept-5-en-2-ol dissolved in 100 ml diethyl ether were droppered into the reaction solution at 0° C. Once addition was complete stirring continued for a further hour at 0° C. followed by heating to room temperature. Once the reaction solution had been stirred for 12 hours at room temperature, quenching was carried out with saturated ammonium chloride solution (500 ml) and following conditioning of the raw product obtained distillation was performed via a 30 cm packed column. 82 g of 2,2,6-trimethyl-5-isopropenyltetrahydropyran with a purity of 98% were obtained (55% of theoretical yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08242289B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-4430f0f9d19c460b8f03ee52d92cc6a6 |
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| Source note | uspto-grants-2012_08 |
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