HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 332578Generated: October 25, 2026
N,N-Dimethylglycine → 3-(5-Formyl-2-methoxy-phenoxy)-benzonitrile
https://huagongshe.com/reaction/332578
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-Dimethylglycine | HCID 673 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Isovanillin | HCID 12127 | — |
| Reactant | 3-Iodobenzonitrile | HCID 144341 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-(5-Formyl-2-methoxy-phenoxy)-benzonitrile | HCID 57701126 | 43.7% |
Reaction Steps
In a 350 mL pressure vessel equipped with a stir bar was placed 3-hydroxy-4-methoxy-benzaldehyde (15) (1.5 g, 9.86 mmol), 3-iodo-benzonitrile (3.39 g, 14.8 mmol), cesium carbonate (3.21 g, 9.86 mmol), N,N-dimethylglycine (275 mg, 1.97 mmol), copper(I) iodide (188 mg, 0.986 mmol) and 1,4-dioxane (55 mL). The mixture was heated to 100° C. for 46 hours. The reaction was cooled to room temperature, quenched with water (300 mL) and then extracted with ethyl acetate (3×200 mL). The organic portions were combined, washed with brine (300 mL), dried (MgSO4) and concentrated. The crude material was purified by silica gel column chromatography utilizing 35%, 50%, 75% ethyl acetate/hexanes to produce 1.09 g (42% yield) of (16) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08877816B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-7a2fe04db1af45a7a321260c6f33f946 |
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| Source note | uspto-grants-2014_11 |
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