HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 229935Generated: October 29, 2026
Dimethylformamide → 2-Difluoromethoxy-6-propylsulfanylbenzonitrile
https://huagongshe.com/reaction/229935
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Propyl mercaptan | HCID 7848 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-(Difluoromethoxy)-6-fluorobenzonitrile | HCID 23448361 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Difluoromethoxy-6-propylsulfanylbenzonitrile | HCID 68565116 | 76% |
Reaction Steps
180 g (0.96 mol) 2-difluoromethoxy-6-fluorobenzonitrile were introduced into 1.5 l of dimethylformamide at room temperature. 73.2 g (0.96 mol) of propanethiol were added dropwise and, after cooling to 0° C., 70 g (1.25 mol) of potassium hydroxide pellets, dissolved in 600 ml of water, were added dropwise at 0° C. The mixture was stirred for one hour and then warmed to room temperature. The reaction mixture was stirred into 3.5 l of ice-water and extracted three times with 500 ml of methyl tert.-butyl ether. The combined organic phases were washed twice with 500 ml of 1N hydrochloric acid and dried over sodium sulfate. Then, the solvent was distilled off in vacuo. The oil obtained was distilled in vacuo (b.p.: 180-185° C./0.5 mbar). Yield: 76% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07563921B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-9eef223353e64379bcb80fd4f526eb3d |
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| Source note | uspto-grants-2009_07 |
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