HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172351Generated: November 3, 2026
2,4-Dimethyl-3-cyclohexene carboxaldehyde → α-Ethyl-2,4-dimethyl-3-cyclohexene-1-methanol
https://huagongshe.com/reaction/2172351
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,4-Dimethyl-3-cyclohexene carboxaldehyde | HCID 93375 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | α-Ethyl-2,4-dimethyl-3-cyclohexene-1-methanol | HCID 118112370 | — |
Reaction Steps
A reaction flask was charged with ethylmagnesium bromide solution (CH3CH2MgBr) (3 M, 2.4 L) in tetrahydrofuran (THF) and cooled to 0° C. 2,4-Dimethyl-cyclohex-3-enecarbaldehyde (905 g) was added slowly while the temperature was kept at 0° C. The reaction mixture was stirred for an additional hour and then quenched with hydrochloric acid (HCl). The reaction mixture was washed with sodium carbonate (Na2CO3) and brine. Further distillation provided 1-(2,4 -dimethyl-cyclohex-3-enyl)-propan-1-ol (1.021 Kg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051532B1 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-0578cbaaf9d64da2a017477a06e2d6f4 |
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| Source note | uspto-grants-2015_06 |
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