HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2407466Generated: October 31, 2026
Ammonium Chloride → (4-Bromophenyl)(cyclopropyl)methanol
https://huagongshe.com/reaction/2407466
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-Bromobenzaldehyde | HCID 70741 | — |
| Reactant | Bromocyclopropane | HCID 78037 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4-Bromophenyl)(cyclopropyl)methanol | HCID 123566 | — |
| Product | HCID 178418630 | HCID 178418630 | — |
Reaction Steps
Solution of cyclopropyl magnesium bromide is prepared from cyclopropyl bromide (12 g, 0.099 mol) and magnesium turnings (3.0 g, 0.123 mol) in tetrahydrofuran (60 mL) by using standard Grignard reaction procedure. This reagent solution is cooled to 5° C. and a solution of 4-bromobenzaldehyde (15.0 g, 0.081 mol) in tetrahydrofuran (30 mL) is added to it over a period of 15 minute at 10-15° C. The reaction mixture is treated with aqueous ammonium chloride solution and extracted with ethyl acetate (50 mL). The organic layer is concentrated under reduced pressure and the residue is purified by column chromatography (silica gel 230-400 mesh) to give (4-bromophenyl)-cyclopropylmethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08809539B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-a9f351773ab4489db23c7d916144ab73 |
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| Source note | uspto-grants-2014_08 |
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