Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | 2-Ethylhex-2-Enal | HCID 12582 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Product | HCID 11217378 | HCID 11217378 | — |
| Product | HCID 53806099 | HCID 53806099 | — |
Reaction Steps
To a mixture of 28.7 g of 2-ethyl-2-hexenal (purity: 99.0%, 0.225 mol), 12.5 g (0.15 mol) of 37% formalin, and 25 ml of methanol heated to 50° C. was added dropwise 3.37 g (0.015 mol) of a 25% aqueous solution of potassium hydroxide over 20 minutes. After the dropping was completed, the mixture was further stirred at 50° C. for 4 hours. The reaction mixture was analyzed by gas chromatography (the internal standard method with diethylene glycol dimethyl ether as an internal standard), and the yields of 2,4-diethyl-5-hydroxy-2-pentenal and 3,5-diethyl-5,6-dihydro-2H-2-pyranol based on the used formaldehyde and the consumed 2-ethyl-2-hexenal were found to be as follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06072089 |
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| Source dataset | uspto-grants-2000_06 |
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| ORD ID | ord-9b080ac02458495a96691e5456611665 |
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| Source note | uspto-grants-2000_06 |
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