HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361471Generated: October 27, 2026
Potassium Hydroxide → 1-Bromo-4-(cyclopropylmethyl)benzene
https://huagongshe.com/reaction/361471
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 4-Bromophenyl cyclopropyl ketone | HCID 81394 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Product | 1-Bromo-4-(cyclopropylmethyl)benzene | HCID 11651397 | 49.2% |
Reaction Steps
4-Bromophenyl cyclopropyl ketone (5.63 g), hydrazine monohydrate (2.5 ml) and potassium hydroxide (3.33 g) were added to ethylene glycol (25 ml) and the mixture heated to reflux for 1 hour. The reaction mixture was cooled and partitioned between water (20 ml) and ethyl acetate (30 ml) and the organic layer was separated. The aqueous layer was extracted with ethyl acetate (30 ml) and the combined organic phases were washed with 2M hydrochloric acid (15 ml) and water (15 ml) then dried (MgSO4) and evaporated. The residue was purified by chromatography on a Mega Bond Elut column, eluting with hexane to give 1-bromo-4-(cyclopropylmethyl)benzene (2.6 g); 1H NMR (CDCl3): 0.2 (m, 2 H), 0.55 (m, 2 H), 2.50 (d, 2 H), 7.14 (d, 2 H), 7.41 (d, 2 H); mass spectrum (EI+) 210 (M.)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05866568 |
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| Source dataset | uspto-grants-1999_02 |
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| ORD ID | ord-a955da66795b45b6b9a20c28ddf95d80 |
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| Source note | uspto-grants-1999_02 |
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