HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980504Generated: October 30, 2026
p-Bromochlorobenzene → HCID 12501054, compound
https://huagongshe.com/reaction/1980504
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Bromochlorobenzene | HCID 7806 | — |
| Reactant | HCID 57370169 | HCID 57370169 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Lithium Chloride | HCID 433294 | — |
| Product | HCID 12501054 | HCID 12501054 | 12% |
Reaction Steps
A solution of 14.4 g (0.075 mol) of 4-bromochlorobenzene and 9.5 ml (12.3 g, 0.075 mol) of chloromethyl(dichloro)methylsilane in 150 ml of tetrahydrofuran was cooled to -60° under nitrogen and stirred while 94 ml (0.15 mol) of 1.6 molar n-butyllithium in hexane was added dropwise at a rate that held the mixture between -65° and -55°. The resulting slurry was allowed to warm to room temperature, giving a solution that was diluted with hexanes until no more lithium chloride precipitated. Filtration, evaporation of the filtrate, dissolution of the residue in hexanes, refiltration, and evaporation left 19.8 g of a pale orange liquid. Distillation gave first 1.8 g (12%) of chloromethyl(dibutyl)methylsilane, bp 45° C. (0.05 mm), followed by 6.8 g (35%) of the title compound as a colorless liquid: bp 90° C. (0.05 mm); nD21 1.5246; ir (neat) 2925, 1580, 1380, 1260, 1090, 1015, 820, 740 cm-1 ; nmr (CDCl3) 0.4 (3H, s), 0.6-1.5 (9H, m), 2.9 (2H, s), 7.0-7.4 (4H, q).
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-c0d1f7c977d54dd5aaf8e935780b717c |
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| Source note | uspto-grants-1985_04 |
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