HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 861930Generated: October 30, 2026
Water → 7-Amino-5-cyano-8-methylquinoline
https://huagongshe.com/reaction/861930
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 1,1,3-Trimethoxypropane | HCID 84348 | — |
| Reactant | 3,5-Diamino-4-methylbenzonitrile | HCID 18465375 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 7-Amino-5-cyano-8-methylquinoline | HCID 18465380 | — |
Reaction Steps
A mixture of 4-cyano-2,6-diaminotoluene (3.56 g), ferric chloride hexahydrate (11.63 g), and zinc chloride (0.499 g) in ethanol (600 mL) is warmed to 65° C. A solution of 1,1,3-trimethoxypropane (5.23 g) in ethanol (90 mL) is added dropwise via syringe pump over a period of 90 minutes. The reaction is then heated to reflux for 2.5 hours. The reaction is cooled to room temperature and the solvent rotary evaporated. The residue is mixed with 300 mL of water and basified to pH=11 with concentrated ammonium hydroxide. The products are extracted with ethyl acetate (4×300 mL), and the combined extracts dried over sodium sulfate and rotary evaporated. The residue is purified by flash chromatography on silica gel, eluting with 50% ethyl acetate/hexane to afford 7-amino-5-cyano-8-methylquinoline as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05716966 |
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| Source dataset | uspto-grants-1998_02 |
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| ORD ID | ord-b3c062489e254280a1fbe59b92f0f98a |
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| Source note | uspto-grants-1998_02 |
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