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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 924622Generated: October 30, 2026

Formaldehyde → 4-Ethenyl-1-cyclohexene-1-carboxaldehyde

https://huagongshe.com/reaction/924622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant1,3-ButadieneHCID 7845—
ReactantCrotonaldehydeHCID 447466—
CatalystPropionic AcidHCID 1032—
CatalystPyrrolidineHCID 31268—
SolventDimethylformamideHCID 6228—
Product1-Ethenyl-3-cyclohexene-1-carboxaldehydeHCID 89525526—
Product4-Ethenyl-1-cyclohexene-1-carboxaldehydeHCID 8971499593%

Reaction Conditions

Temperature100 °C

Reaction Steps

The 500 mL flask was charged with crotonaldehyde (210.3 g, 3 mol), formaldehyde (270.0 g, 3.24 mol, 36% aqueous solution) and DMF (50 g, 0.68 mol). A cooled mixture of pyrrolidine (5.33 g, 0.075 mol) and propionic acid (5.56 g, 0.075 mol) was added with stirring during 5 minutes. This combined mixture was then slowly pumped with stirring into a heated (100° C.) autoclave that had been charged with a solution of 1,3-butadiene (570.4 g, 5 mol) in DMF (250 g, 3.42 mol). (Careful: a cold autoclave has to be charged with a cooled solution of butadiene in DMF, boiling point of butadiene: −4.5° C.). At this temperature, the internal pressure was 12.0 bar. During the first 3 h of this addition, the internal pressure slowly rose to 14.5 bar, while the temperature was kept at 100° C. The pressure then slowly dropped to 11.0 bar until the addition was finished after 4.5 hours. The reaction mixture was stirred at 100° C. for another 2 hours. After that time (the pressure was less than 8.1 bar) the reaction mixture was cooled to room temperature (by means of an internal cooling device) upon which the internal pressure dropped to less than 2 bar. The mixture was transferred to a 2.0 L separation funnel and diluted with hexane (620 g) and water (300 g) (Careful: excessive butadiene evaporates during this operation: use well ventilated hood). The upper layer was separated and washed successively with aq. acetic acid (50 ml) and water (50 ml) and then with sat. aq. sodium bicarbonate solution. The organic phase was dried with MgSO4, filtered and concentrated under reduced pressure to furnish the crude product as a yellow oil (254 g) which was then distilled in vacuo over a 10 cm-Vigreux column (b.p. 47-72° C., 0.1 mbar), to yield 1-vinylcyclohex-3-ene carbaldehyde and 4-vinylcyclohex-1-ene carbaldehyde (189.9 g, 46.5%) in a ratio of about 2:1. The compounds may be separated by distillation or chromatography on silica gel under conditions known to the skilled person.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09283159B2
Source datasetuspto-grants-2016_03
ORD IDord-68934788d2534274a1395b27f3cad4a1
Source noteuspto-grants-2016_03