HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533510Generated: October 31, 2026
Sodium Cyanide → 2-(4-Bromo-2-methylphenyl)acetonitrile
https://huagongshe.com/reaction/533510
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 4-Bromo-1-(chloromethyl)-2-methylbenzene | HCID 20072358 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(4-Bromo-2-methylphenyl)acetonitrile | HCID 18414296 | 98% |
Reaction Steps
4-Bromo-1-chloromethyl-2-methyl-benzene (63 g, 287 mmol) was dissolved in DMF (180 mL). NaCN (15.5 g, 316 mmol, 1.1 eq.) was added in 1 portion, and the reaction was stirred at room temperature overnight under a N2 atmosphere. The mixture was concentrated under reduced pressure, and the residue was taken into a mixture of sat. aq. NH4Cl (300 mL) and EtOAc (300 mL). The bi-phase solution was diluted with H2O (200 mL). The EtOAc layer was separated, and the aqueous layer was re-extracted with EtOAc (2×200 mL). The combined organic layers were washed with brine (3×300 mL), dried (Na2SO4), filtered, and concentrated under reduced pressure, yielding the title compound (58.8 g, 280 mmol, 98%) with acceptable purity as a brown oil, which solidified to a brown solid on standing. 1H-NMR (CDCl3, 300 MHz) δ ppm 2.34 (s, 3H); 3.63 (s, 2H); 7.26 (t, 1H); 7.38 (d, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853258B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-c70531bebcb44fb4a0a5c11efdec709b |
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| Source note | uspto-grants-2014_10 |
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