HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2052536Generated: October 31, 2026
Dimethylformamide → 1-(1-Bromoethyl)-3-(trifluoromethyl)benzene
https://huagongshe.com/reaction/2052536
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 1-(3-(Trifluoromethyl)phenyl)ethanol | HCID 136296 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 1-(1-Bromoethyl)-3-(trifluoromethyl)benzene | HCID 2775624 | — |
Reaction Steps
bromine (32.5 g≡10.4 ml) was added over 15 minutes to a stirred mixture of (±)-1-(3-trifluoromethylphenyl)-ethanol [38 g, described by Overberger et al., Org. Synth. Coll. 3, 200 (1955)], triphenylphosphine (56 g) and dry dimethylformamide (200 ml) in an atmosphere of nitrogen. The temperature of the mixture was maintained at 40°-50° C. by ice-cooling. Further bromine was added dropwise to give a permanent orange colour and after stirring for 15 minutes the mixture was poured into a mixture of ice-water (1 liter) and hexane (500 ml). The mixture was filtered and the solid material was washed well with hexane. The hexane solutions were combined, washed with water (4×100 ml), dried over sodium sulphate and distilled to give (±)-1-(3-trifluoromethylphenyl)ethyl bromide, b.p. 98°-105° C./15 mmHg, as a clear mobile oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04185992 |
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| Source dataset | uspto-grants-1980_01 |
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| ORD ID | ord-47dece557f104bd18203dc965fcc4074 |
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| Source note | uspto-grants-1980_01 |
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