HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 603142Generated: October 30, 2026
Ammonia → 2-[4-(Aminomethyl)-3-methylphenyl]-2-methylpropanenitrile
https://huagongshe.com/reaction/603142
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-(4-Formyl-3-methylphenyl)-2-methylpropanenitrile | HCID 58298453 | — |
| Catalyst | HCID 178460666 | HCID 178460666 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-[4-(Aminomethyl)-3-methylphenyl]-2-methylpropanenitrile | HCID 58298448 | 87% |
Reaction Steps
2-(4-formyl-3-methylphenyl)-2-methylpropanenitrile 1.89 g, 10.2 mmol) is dissolved in 50 ml of 7M NH3 in MeOH. Ti(OiPr)4 (6 mmol, 20 mmol) is added and the mixture stirred for 3 hours at room temperature. NaBH4 (0.6 g, 15 mmol) is added and the reaction left at room temperature overnight. The mixture is quenched by the addition of 25 ml of NH4OH 2 M. The resulting precipitate is filtered off and washed with EtOAc. Phases are separated, the organic phase is dried over magnesium sulfate, filtered and evaporated to dryness, giving 2-[4-(aminomethyl)-3-methylphenyl]-2-methylpropanenitrile (1.325 g, 7.09 mmol, 87%). The crude product is used without further purification. 1H NMR (400 MHz, DMSO-D6) δ 1.64 (s, 6H, first rotamer) 1.65 (s, 6H, second rotamer) 2.28 (s, 3H, first rotamer) 2.29 (s, 3H, second rotamer) 3.32 (broad s, 2H) 3.67 (s, 2H, first rotamer) 3.68 (s, 2H, second rotamer) 7.24-7.27 (m, 1H) 7.28 (s, 1H) 7.36-7.40 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07906654B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-d137a0f6c75b4178ba2e7bbd98549db7 |
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| Source note | uspto-grants-2011_03 |
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