HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 893293Generated: October 28, 2026
p-Bromochlorobenzene → HCID 2757630, compound
https://huagongshe.com/reaction/893293
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Bromochlorobenzene | HCID 7806 | — |
| Reactant | 3-Methoxybenzaldehyde | HCID 11569 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 2757630 | HCID 2757630 | 99.3% |
Reaction Steps
A solution of 35.0 g (183 mmole) of 4-bromochlorobenzene in 300 ml of dry tetrahydrofuran was cooled to -78° C. under nitrogen and 115 ml (183 mmole) of 1.59 M n-butyllithium in hexane was added dropwise at a rate to maintain temperature below -60° C. After stirring an additional 15 minutes, 23.0 ml (183 mmole) of m-anisaldehyde was added dropwise and the reaction was stirred for 15 minutes. The reaction was quenched at -78° C. with saturated aqueous ammonium chloride and allowed to warm to room temperature. The reaction solution was diluted with 300 ml of diethyl ether and washed with three 150 ml portions of 1.0 M sodium bisulfite, followed by 100 ml of 1.0 M sodium hydroxide, 100 ml of water, and 50 ml of saturated sodium chloride. After drying over magnesium sulfate, the solvent was removed to give 45.2 g (99%) of crude 4-chloro-α-(3-methoxyphenyl)benzyl alcohol as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05124330 |
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| Source dataset | uspto-grants-1992_06 |
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| ORD ID | ord-08472abb45e149de8918a6b4eacea8c0 |
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| Source note | uspto-grants-1992_06 |
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