HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499002Generated: October 26, 2026
Methylamine → [5-Bromo-2-(3,4-dichloro-phenoxy)-benzyl]-methyl-amine
https://huagongshe.com/reaction/499002
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-Bromo-2-(3,4-dichlorophenoxy)benzaldehyde | HCID 12017030 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | [5-Bromo-2-(3,4-dichloro-phenoxy)-benzyl]-methyl-amine | HCID 9947009 | 97% |
Reaction Steps
To a mixture of 5-bromo-2-(3,4-dichloro-phenoxy)-benzaldehyde (4.74 g, 13.8 mmol) in MeOH (250 mL) was added MeNH2 (40% aq.; 20 mL, 260 mmol), and the resulting mixture was stirred at rt until homogeneous. The mixture was cooled to 0° C. and treated with NaBH4 (1.05 g, 27.8 mmol) portionwise. After 24 h, the mixture was concentrated and the residue was diluted with 1 N NaOH and extracted with DCM. The combined organic layers were dried (Na2SO4) and concentrated. The crude product was purified by FCC to provide the desired product (4.80 g, 97%). MS (ESI): mass calcd. for C14H12BrCl2NO, 358.95; m/z found, 360.1 [M+H]+. 1H NMR (CDCl3): 7.61 (d, J=2.5, 1H), 7.40-7.37 (m, 2H), 7.03 (d, J=2.8, 1H), 6.82-6.79 (m, 2H), 3.72 (s, 2H), 2.44 (s, 3H), 1.30-1.21 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07767666B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-3ae549d54a8b415bbc522d5b18171081 |
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| Source note | uspto-grants-2010_08 |
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