HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837420Generated: November 4, 2026
Formaldehyde → 6-Methyl-3-cyclohexene-1,1-dimethanol
https://huagongshe.com/reaction/1837420
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 1,3-Butadiene | HCID 7845 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 6-Methyl-3-cyclohexene-1-carboxaldehyde | HCID 101550 | — |
| Reactant | Crotonaldehyde | HCID 447466 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Methyl-3-cyclohexene-1,1-dimethanol | HCID 138997 | 82% |
Reaction Steps
To a three-necked flask, 327 g of 2-methyl-4-cyclohexene-1-carboaldehyde, a Diels-Alder reaction product of butadiene and crotonaldehyde, 600 ml of methanol and 729 g of 37% of formalin were charged, and then the temperature of this solution was raised to 60° C. with stirring. Next, 252 g of KOH dissolved in 600 ml of distilled water was added dropwise thereto. After stirring for 7 hours, the reaction solution was concentrated under reduced pressure, which resulted in a residue with two phases. The oil phase concentrated to about 150 ml was washed with 300 ml of distilled water. After concentration under reduced pressure, 50 mg of 3,5-di(t-butyl)-4-hydroxytoluene (BHT) was added to the oil phase, and then vacuum distillation was carried out to yield 311 g (yield 82%) of 6-methyl-3-cyclohexene-1,1-dimethanol as a colorless crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06783840B2 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-e38855075db9499d8eb7bccfe03858b1 |
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| Source note | uspto-grants-2004_08 |
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