HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269250Generated: October 31, 2026
Dimethylformamide → 3-Cyano-4-(trifluoromethoxy)benzaldehyde
https://huagongshe.com/reaction/2269250
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 3-Iodo-4-(trifluoromethoxy)benzaldehyde | HCID 18333619 | — |
| Catalyst | Zinc cyanide (Zn(CN)2) | HCID 11186 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-Cyano-4-(trifluoromethoxy)benzaldehyde | HCID 18677603 | — |
Reaction Steps
To a stirred suspension of Compound 19 (6.85 g, 21.7 mmol) and zinc cyanide (4.07 g, 34.7 mmol) in dry DMF (35 ml) was added tetrakis(triphenylphosphine)palladium(0) (3.00 g, 2.60 mmol) portionwise at room temperature. The reaction mixture was heated at 100° C. for 9 h. The reaction mixture was diluted with toluene (100 ml)-2M NH3 aq. (100 ml). The organic layer was separated. The aqueous layer was diluted with toluene (100 ml), filtered through a pad of celite and the filter cake was washed with toluene. The organic layer was separated and the aqueous layer was extracted with toluene. The combined solution was washed with 2M NH3 aq. (50 ml) and brine, dried (MgSO4), and concentrated in vacuo to give crude product as a dark tan oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06329396B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-88542c3d4a20409d8e1c9aed903c1f7c |
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| Source note | uspto-grants-2001_12 |
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