HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032908Generated: October 30, 2026
1,2-Dimethoxyethane → HCID 131718398, compound
https://huagongshe.com/reaction/1032908
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | o-(Trifluoromethyl)benzaldehyde | HCID 123067 | — |
| Reactant | 2-Chloro-4-(trifluoromethyl)pyridine | HCID 144958 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Product | HCID 131718398 | HCID 131718398 | — |
Reaction Steps
To a 3-neck flask equipped with a dropping funnel, a thermometer, and a condenser with a drying tube were added 5 grams of 2-chloro-4-trifluoromethyl pyridine and 5 ml of ethylene glycol dimethyl ether. The mixture was cooled to -70° C. and 22 ml of LDA were slowly added with the temperature maintained below -55° C. The reaction mixture was stirred at -70° C. for 1.5 hours, and 3.5 ml of 2-trifluoromethyl benzaldehyde added. The reaction mixture was stirred in a dry-ice bath, then at room temperature over night. Fifteen ml of saturated aqueous ammonium chloride solution was added, the solvent stripped and the oil residue washed with water and extracted with methylene chloride (3 times). The combined methylene chloride layers were washed with brine, dried and stripped to yield a brown oil. The brown oil was put onto a silica gel column and eluted with a 1:1 mixture of hexane and diethyl ether to yield 6.2 grams of 2-chloro-3-(1-hydroxy-2'-trifluoromethyl-benzyl)-4-trifluoro methyl-pyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05308826 |
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| Source dataset | uspto-grants-1994_05 |
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| ORD ID | ord-a50b75cfa00e43cb8a4158b66b03efc0 |
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| Source note | uspto-grants-1994_05 |
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