HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604427Generated: November 1, 2026
Potassium Cyanide → (3-Cyclopropylmethoxy-4-methoxyphenyl)acetonitrile
https://huagongshe.com/reaction/1604427
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 4-(Chloromethyl)-2-(cyclopropylmethoxy)-1-methoxybenzene | HCID 22456846 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (3-Cyclopropylmethoxy-4-methoxyphenyl)acetonitrile | HCID 22456848 | 87.4% |
Reaction Steps
A mixture of 4-(chloromethyl)-2-(cyclopropylmethoxy)-1-methoxybenzene (7.4 g) in DMF (68 ml) was stirred at 60° C. A mixture of potassium cyanide (4.26 g) in water (3.4 ml), previously heated to 80° C., was added dropwise. The resulting reaction mixture was stirred for 30 minutes at 60° C. The reaction mixture was cooled, treated with water (47 ml), and extracted with DIPE. The separated organic layer was dried (Na2SO4), filtered, and the solvent was evaporated, yielding 6.2 g (85%) of 3-(cyclopropylmethoxy)-4-methoxybenzeneacetonitrile (interm. 16).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05994376 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-a373fde82e514c5daaf7e7bbffdf488e |
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| Source note | uspto-grants-1999_11 |
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