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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852324Generated: November 2, 2026

Octyl cyanoacetate → HCID 86678045, compound

https://huagongshe.com/reaction/1852324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOctyl cyanoacetateHCID 4384482—
ReactantHCID 86678046HCID 86678046—
ReactantHCID 86678047HCID 86678047—
SolventAcetic AnhydrideHCID 7918—
ProductHCID 86678045HCID 8667804579%

Reaction Steps

3-Anilinoacrolein-aniline (27.7 g, 0.125 mol) and n-octyl cyanoacetate (26.3 ml, 0.125 mol) are heated in 70 ml of acetic anhydride at 115° C. for 2 hours while bubbling with nitrogen. After cooling, 80 ml of methanol are added and precipitation is allowed to take place. The solid obtained is filtered off and rinsed with methanol. Drying is carried out. 36.4 g of a yellow powder (yield: 79%) of butyl (2E,4E)-5-[acetyl(phenyl)amino]-2-cyanopenta-2,4-dienoate are recovered, which powder is used as is in the following stage.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08961941B2
Source datasetuspto-grants-2015_02
ORD IDord-37844cefff924f919cc756a4081d5af5
Source noteuspto-grants-2015_02