HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752590Generated: October 28, 2026
Bromoacetonitrile → 2-((4-Methoxybenzyl)amino)acetonitrile
https://huagongshe.com/reaction/1752590
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromoacetonitrile | HCID 11534 | — |
| Reactant | 4-Methoxybenzylamine | HCID 75452 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-((4-Methoxybenzyl)amino)acetonitrile | HCID 9989760 | 76.4% |
Reaction Steps
A mixture of TEA (55.9 ml, 401 mmol), (4-methoxyphenyl)methanamine (50 g, 364 mmol) and 2-bromoacetonitrile (43.7 g, 364 mmol) in THF (500 ml) was stirred at about 10° C. for about 12 h in a 500 ml round-bottomed flask. The reaction was filtered through a pad of silica gel. The crude material was deposited onto silica gel, loaded onto a silica gel column and eluted with Hex/EtOAc (1:1) to afford the title compound (49 g, 278 mmol, 76% yield). 1H-NMR (CDCl3, 400 MHz): δ=3.55 (s, 2H), 3.81 (s, 3H), 3.87 (s, 2H), 6.88 (d, 2H, J=8.4 Hz), 7.26 (d, 2H, J=8.0 Hz)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09163019B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-8f4b9b68f17c4005b81569c65bb257ad |
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| Source note | uspto-grants-2015_10 |
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