HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N-Dimethylaniline → 6-Bromo-N-(3,5-dichloro-4-hydroxyphenyl)hexanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | 4-Amino-2,6-dichlorophenol | HCID 80037 | — |
| Reactant | 6-Bromohexanoyl chloride | HCID 89848 | — |
| Product | 6-Bromo-N-(3,5-dichloro-4-hydroxyphenyl)hexanamide | HCID 14500510 | 89% |
Reaction Steps
was prepared in 89% yield from 24.4 g (0.14 mol) of 4-amino-2,6-dichlorophenol, 18.1 g (0.15 mol) of N,N-dimethylaniline and 28.8 g (0.14 mol) of 6-bromohexanoyl chloride according to the procedure of Example 6, part a, except that the reaction was cooled on ice during the addition and was stirred at room temperature rather than refluxed. The product was crystallized from ethanol-water, mp 113°-114° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04835180 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-9a8ad80af68d4f1ba775d67826b01cab |
| Source note | uspto-grants-1989_05 |