HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propanoyl bromide, 2-bromo- → 2-Bromo-N-(4-butoxy-2,6-dimethylphenyl)propanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propanoyl bromide, 2-bromo- | HCID 79047 | — |
| Reactant | HCID 12546818 | HCID 12546818 | — |
| Reactant | Sodium Acetate Trihydrate | HCID 23665404 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Bromo-N-(4-butoxy-2,6-dimethylphenyl)propanamide | HCID 12546828 | — |
Reaction Steps
To a chilled (ca 10°) solution of 50.7 g (0.263 mole) of 4-butoxy-2,6-dimethylaniline [Buchi et al., Helv. Chim. Acta, 34, 278 (1951) ] in 224 ml glacial acetic acid was added rapidly 62.4 g (.289 mole) of 2-bromo-propionyl bromide and immediately thereafter a chilled (ca 5°) solution of 87.2 g sodium acetate trihydrate in 362 ml water. This mixture was shaken for 1/2 hour, filtered, washed with water until the washes were neutral, and dried in vacuo over silica gel and KOH; yield 68.9 g (71.6%); m.p. 132.5° - 133.5°. The product was recrystallized from 95% ethanol; m.p. 135.5° - 136°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04029794 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-0eaa9da18d5e4e5f87293ff8862db884 |
| Source note | uspto-grants-1977_06 |