HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 86646565, compound → HCID 86646564, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 86646565 | HCID 86646565 | — |
| Reactant | HCID 178418486 | HCID 178418486 | — |
| Product | HCID 86646564 | HCID 86646564 | — |
Reaction Steps
In a manner analogous to example 1 e, the process is carried out by a reaction of 800 mg (3 mmol) of 3-tert-butyl-4-(ethylisobutylamino)benzaldehyde with 8 ml (4 mmol) of a 0.5M solution of ethynylmagnesium bromide. 700 mg of 1-[3-tert-butyl-4-(ethylisobutyl-amino)phenyl]prop-2-yn-1-ol are obtained in the form of a colourless oil (yield=81%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08163952B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-1b2ee3cd285d49559cf51f7da37eb4d6 |
| Source note | uspto-grants-2012_04 |