HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1883637Generated: November 2, 2026
2-Methyl-5-phenylbenzonitrile → 2-Methyl-5-phenylbenzylamine
https://huagongshe.com/reaction/1883637
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methyl-5-phenylbenzonitrile | HCID 11171537 | — |
| Reactant | Azane;hydrate | HCID 12896473 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-Methyl-5-phenylbenzylamine | HCID 23508213 | 82.6% |
Reaction Steps
1.0 g (5.17 mmol) of 2-methyl-5-phenylbenzonitrile (produced in the same manner as in the above-mentioned Reference Production Example 1 (2)) was dissolved in a mixed solvent of 8 ml of 1,4-dioxane and 8 ml of ethanol, and to this solution was added 1.0 g of a suspension of 2 ml of 28 wt % ammonia water and Raney nickel W2 (manufactured by Aldrich; 50 wt % in water). This mixture was stirred for 8 hours at room temperature under hydrogen atmosphere, then, filtrated through celite, and the celite was washed with ethanol and water. The filtrate and washed solution was combined and concentrated under reduced pressure, and the residue was distilled by using Kugelrohl distillation apparatus (0.5 mmHg, set temperature: 216° C.), to obtain 842 mg (4.27 mmol) of 2-methyl-5-phenylbenzylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06762197B2 |
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| Source dataset | uspto-grants-2004_07 |
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| ORD ID | ord-9b56c1dae3c44bddac9e06defce4dde5 |
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| Source note | uspto-grants-2004_07 |
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