HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927308Generated: October 26, 2026
Diethyl Ether → 1-(2-Bromo-3-chloro phenyl)butan-1-ol
https://huagongshe.com/reaction/1927308
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Bromo-3-chlorobenzaldehyde | HCID 23463927 | — |
| Reactant | HCID 178455855 | HCID 178455855 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(2-Bromo-3-chloro phenyl)butan-1-ol | HCID 58572792 | 62% |
Reaction Steps
Under an argon atmosphere, zinc chloride (0.68 g, 4.97 mmol) was added to a 2.0 M solution of n-propyl magnesium chloride in diethyl ether (12.42 mL, 24.93 mmol), and the mixture was stirred at room temperature. After stirring for 0.5 hours, a solution of 2-bromo-3-chlorobenzaldehyde (4.36 g, 19.87 mmol), which had been obtained in Reference example 5(5b), in tetrahydrofuran (10 mL) was added dropwise thereto. After stirring for 2 hours under ice cooling, a saturated aqueous ammonium chloride solution (20 mL) was added thereto. The mixture obtained was extracted with ethyl acetate (20 mL×2). After that, the organic layers were washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (n-hexane/ethyl acetate=5/1) to give the title compound as a white solid (3.23 g, yield 62%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08183272B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-264ffd6ae3e64b41afe54be4725e45df |
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| Source note | uspto-grants-2012_05 |
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