HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → HCID 23316556, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,4,6-Trichloroaniline | HCID 12471 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Product | HCID 23316556 | HCID 23316556 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
2,4,6-trichloroaniline, 49.1 gm, was added to 250 ml of methylene chloride. The system was cooled to 0° C. and 34.8 ml of triethylamine was then added. After addition of the triethylamine, 21.8 ml of bromacetylbromide was added. The system was allowed to warm to room temperature and stirred there for 18 hours. The reaction was then stopped and the solvent was washed with saturated sodium bicarbonate solution. The methylene chloride layer was separated and partially stripped when a solid precipitated from solution. The solid was filtered and air dried to yield 41.4 gm of α-bromo-(2,4,6-trichlorophenyl) acetamide as a gray solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04532251 |
| Source dataset | uspto-grants-1985_07 |
| ORD ID | ord-3e12e3bb66724909bb7008c9152e63f1 |
| Source note | uspto-grants-1985_07 |