HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,5-Di-tert-butyl-4-hydroxybenzaldehyde → (E)-3-(3,5-Di-t-butyl-4-hydroxyphenyl)-2-[(3-phenyl-n-propyl)aminosulfonyl]acrylonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,5-Di-tert-butyl-4-hydroxybenzaldehyde | HCID 73219 | — |
| Reactant | (3-Phenyl-n-propyl)aminosulfonylacetonitrile | HCID 15410494 | — |
| Product | (E)-3-(3,5-Di-t-butyl-4-hydroxyphenyl)-2-[(3-phenyl-n-propyl)aminosulfonyl]acrylonitrile | HCID 15410491 | — |
Reaction Steps
N-3-Phenyl-n-propyl cyanomethylsulfonamide and 3,5-di-t-butyl-4-hydroxybenzaldehyde was condensed under the similar conditions as described for example 12 (Part B) to yield the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06225346B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-07074389624743beadce5e08e2b4d79e |
| Source note | uspto-grants-2001_05 |