HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene, 1-bromo-3-(trifluoromethyl)- → HCID 20073070, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene, 1-bromo-3-(trifluoromethyl)- | HCID 9817 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 21488089 | HCID 21488089 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 20073070 | HCID 20073070 | — |
Reaction Steps
An ether solution of a Grignard reagent prepared from 50.0 g. (0.35 mole) of 3-bromobenzotrifluoride, 400 ml. of ether and 8.6 g. (0.354 mole) of magnesium was treated at -20°C. to -30°C. with 12.5 g. (0.059 mole) of crude 1-cyclopropyl-3-(N-methyl-acetamido)-1-propanone (calculated to contain 80% of the propanone by the nuclear magnetic resonance spectrum) in 100 ml. of ether. The reaction mixture was warmed to room temperature and treated with 7.4 g. (0.14 mole) ammonium chloride followed by 20 ml. of water. The ether layer was separated, concentrated to a dark oil and distilled under reduced pressure. The yield was 6.2 g.; b.p. 110°-114°C./0.1 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03978130 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-ccaaf382a98d4b4f9cf26ad1e751bdb0 |
| Source note | uspto-grants-1976_08 |