HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980507Generated: November 1, 2026
p-Bromochlorobenzene → HCID 131714090, compound
https://huagongshe.com/reaction/1980507
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Bromochlorobenzene | HCID 7806 | — |
| Reactant | 1-Bromo-2-chlorobenzene | HCID 12754 | — |
| Reactant | HCID 57370169 | HCID 57370169 | — |
| Reactant | HCID 178418244 | HCID 178418244 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 131714090 | HCID 131714090 | 95% |
Reaction Steps
A solution of 6.3 ml (8.2 g, 0.05 mol) of chloromethyl(dichloro)methylsilane and 8.1 g (0.05 mol) of 2-bromochlorobenzene in 75 ml of dry tetrahydrofuran was chilled to -60° under N2 and stirred while 31 ml (0.05 mol) of 1.6 molar n-butyllithiumhexane solution was added at a rate that held the mixture below -55°. With continued cooling and stirring, 8.1 g (0.05 mol) of 4-bromochlorobenzene was added as a solid, followed by another 31 ml portion of the 1.6 molar n-butyllithium solution at a rate that held the mixture below -55° C. The resulting thin slurry was allowed to warm to room temperature, treated cautiously with 10 ml of ethyl acetate, and worked up as in Example 8 to give 15.0 g of a clear yellow oil. Distillation provided 5.9 g (37%) of the title compound: bp 150°-165° (0.7 mm); nD20 1.5916; ir (neat) 3060, 3020, 2960, 2920, 2870, 1580, 1560, 1490, 1420, 1380, 1255, 1125, 1115, 1085, 1035, 1015, 805, 750 cm-1 ; nmr (CDCl3) 0.8 (3H, s), 3.3 (2H, s), 7.2-7.7 (8H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04510136 |
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| Source dataset | uspto-grants-1985_04 |
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| ORD ID | ord-0c7ade39782f4c489410a7f9b31f2606 |
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| Source note | uspto-grants-1985_04 |
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