HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612230Generated: November 1, 2026
Glycol monoethyl ether → HCID 22466670, compound
https://huagongshe.com/reaction/612230
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Glycol monoethyl ether | HCID 8076 | — |
| Reactant | 4-Chloro-3-(trifluoromethyl)aniline | HCID 67574 | — |
| Reactant | Pyridinium chloride | HCID 10176127 | — |
| Reactant | 4-Chloro-6,7-dimethoxy-quinoline-3-carbonitrile | HCID 10586676 | — |
| Product | HCID 22466670 | HCID 22466670 | 65.5% |
Reaction Steps
A mixture of 0.248 g (1 mmol)of 4-chloro-6,7-dimethoxy-quinoline-3-carbonitrile, 0.215 g of 4-chloro-3-trifluoromethylaniline, 0.116 g (1 mmol) pyridine hydrochloride and 12 ml of 2-ethoxyethanol was heated in a 138-140° C. oil bath for 1.5 hours; progress of the reaction was monitored by TLC. When TLC indicated the disappearance of starting material, the reaction was cooled and concentrated in vacuo to a thick oil. To this oil was added 50 ml of water followed by 5 ml of IM NaHCO3, approximately pH 8. The resulting precipitate was collected, washed with water and diethyl ether, and dried in vacuo at 65° C. to give 0.266 g (65.5%) of the desired product as cream crystals. MP 265-267° C.;: mass spectrum (electrospray, m/e,): 408.2(M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06002008 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-83bd155eb88940178e9a45aa72925212 |
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| Source note | uspto-grants-1999_12 |
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