HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 3-Tert-butyl-5-chloro-4-dimethylaminobenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | (4-Bromo-2-tert-butyl-6-chlorophenyl)dimethylamine | HCID 67276978 | — |
| Reactant | HCID 178418244 | HCID 178418244 | — |
| Product | 3-Tert-butyl-5-chloro-4-dimethylaminobenzaldehyde | HCID 86646571 | 98.7% |
Reaction Steps
In a manner analogous to example 1 d, the process is carried out by a reaction of 2.25 ml (5.6 mmol) of 2.5M n-butyllithium/hexane with 1.5 g (5.2 mmol) of (4-bromo-2-tert-butyl-6-chlorophenyl)dimethylamine and 450 μl (5.8 mmol) of dimethylformamide. 1.23 g of 3-tert-butyl-5-chloro-4-dimethylaminobenzaldehyde are obtained in the form of a yellow oil (yield=99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08163952B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-4b0c0a6cd09c4ca0b519ab201739e62d |
| Source note | uspto-grants-2012_04 |