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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dimethyl-3-cyclohexene carboxaldehydeHCID 93375—
ReactantHCID 178418443HCID 178418443—
SolventTetrahydrofuranHCID 8028—
Productα-Ethyl-2,4-dimethyl-3-cyclohexene-1-methanolHCID 118112370—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051532B1
Source datasetuspto-grants-2015_06
ORD IDord-0578cbaaf9d64da2a017477a06e2d6f4
Source noteuspto-grants-2015_06