HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1664142Generated: October 25, 2026
Dichloromethane → (2-Bromo-5-fluorophenyl)hydrazine
https://huagongshe.com/reaction/1664142
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Bromo-5-fluoroaniline | HCID 2773317 | — |
| Reactant | (2-Bromo-5-fluorophenyl)hydrazine hydrochloride | HCID 21069774 | — |
| Solvent | Water | HCID 962 | — |
| Product | (2-Bromo-5-fluorophenyl)hydrazine | HCID 12891829 | — |
Reaction Steps
To a suspension of (2-bromo-5-fluoro-phenyl)-hydrazine hydrochloride (41 g, 0.17 mol; prepared from 2-bromo-5-fluoroaniline by the method described in U.S. Pat. No. 3,959,309 (1976) p-23, and p-48) in water (300 mL) and CH2Cl2 (200 mL) was added 1N—NaOH (200 mL) until the solution was basic. The CH2Cl2 layer was separated and the aqueous portion was further extracted with CH2Cl2 (150 mL). The combined organic extracts were dried (MgSO4), filtered, and concentrated to obtain 33 g (0.16 mol) of the title compound as an off-white powder: HPLC: 0.89 min (AP 97% at 220 nm); 1H NMR (CDCl3, 500 MHz) δ ppm 3.62 (2H, s, NH2), 5.75 (1H, s, NH), 6.37 (1H, m, 5-CH), 6.87 (1H, dd, J=11, 3 Hz, 3-CH), 7.31 (1H, dd, J=8.6, 5.8 Hz, 6-CH); 13C NMR (CDCl3, 125.8 Hz) 8 ppm 100.0 (d, J=29 Hz, 3-CH), 101.4 (d, J=2.9 Hz, 1-C), 106.1 (d, J=23 Hz, 5-CH), 133.1 (d, J=9.6 Hz, 6-CH), 149.1 (d, J=10.6 Hz, 2-C), 163.5 (d, J=244 Hz, 4-CF); LC/MS m/z 205/207 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08039458B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-8c4ebe43465d4a82aa695bbf3f038a81 |
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| Source note | uspto-grants-2011_10 |
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