HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → HCID 178420343, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | 3-Cyclohexene-1-carboxaldehyde | HCID 7508 | — |
| Reactant | HCID 178420344 | HCID 178420344 | — |
| Product | HCID 178420343 | HCID 178420343 | — |
Reaction Steps
Kimpe et al., Tetrahedron, Vol. 53, No. 31, pg. 10803-10816 (1997) shows synthesis of (E)-N-benzylidene-1-(cyclohex-3-en-1-yl)methanamine by condensing cyclohex-3-enecarbaldehyde with benzylamine to give (E)-N-(cyclohex-3-en-1-ylmethylene)-1-phenylmethanamine, followed by an isomerization reaction using potassium tert-butoxide in THF. Resulting isomerized imine is useful as an intermediate for synthesis of agriculture compounds.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08969562B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-c5832404f37344cdba1ea28115df4334 |
| Source note | uspto-grants-2015_03 |