HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198841Generated: November 1, 2026
Dimethyl Sulfoxide → HCID 178442346, compound
https://huagongshe.com/reaction/1198841
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 178442347 | HCID 178442347 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178442346 | HCID 178442346 | — |
Reaction Steps
A solution of 0.94 ml of oxalyl chloride in 25 ml of dry methylene chloride is treated dropwise at -60° C. within 10 minutes with a solution of 1.56 ml of dimethyl sulphoxide in 5 ml of methylene chloride. 2 minutes later the reaction mixture is treated dropwise at -60° C. within 10 minutes with a solution of 3.51 g of 5-hexyl-2-[p-(trans-4-(hydroxymethyl)cyclohexyl)phenyl]pyridine in 10 ml of methylene chloride and stirred at -60° C. for a further 15 minutes. Thereafter, the reaction mixture is treated with 7 ml of triethylamine, left to warm to room temperature and then poured into water and extracted with methylene chloride. The organic phase is washed twice with water, dried over magnesium sulphate and evaporated. The 5-hexyl-2-[p-(trans- -4-formylcyclohexyl)phenyl]pyridine obtained is purified by chromatography on silica gel.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04898455 |
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| Source dataset | uspto-grants-1990_02 |
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| ORD ID | ord-b1bd2313698e44508d80c066bf588e8e |
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| Source note | uspto-grants-1990_02 |
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