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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1259482Generated: October 30, 2026

Acetic Acid → Heptanal, 2-methylene-

https://huagongshe.com/reaction/1259482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantFormaldehydeHCID 712—
ReactantHeptanalHCID 8130—
CatalystDibutylamineHCID 8148—
SolventWaterHCID 962—
ProductHeptanal, 2-methylene-HCID 77776848.9%

Reaction Conditions

Temperature50 °C

Reaction Steps

A 3-L three-neck flask fitted with an overhead stirrer and a condenser was charged with di-n-butylamine (33 g) and acetic acid (31 g). Formaldehyde solution in water (500 mL, 33%) was added and the resulting solution was heated to 50° C. with stirring. Heptanal (500 g) was fed in over about 1.5 hours. A slight exotherm was noticed during the feed. GC analysis showed the consumption of heptanal and the production of 2-methylene heptanal, and a conversion rate of about 95% after the feed was completed. The reaction was cooled to room temperature and the reaction mixture was poured into a separatory funnel and washed once with HCl solution (5%). The organic layer was then washed once with saturated sodium carbonate to provide crude 2-methylene heptanal (553 g), which was loaded into a 2-L stainless steel pressure reactor along with dicyclopentadiene (343 g). The pressure reactor was sealed and heated to 170° C. with stirring for two hours. The reaction was then cooled to room temperature. The resulting crude product was purified by distillation to yield 2-pentylbicyclo[2.2.1]hept-5-ene-2-carbaldehyde (217 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466325B2
Source datasetuspto-grants-2013_06
ORD IDord-7db7c97fe92b461c9ab462a3b7daca86
Source noteuspto-grants-2013_06