HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1274409Generated: November 1, 2026
Dimethyl Sulfoxide → 4-(7-Chloroquinolin-4-yl)butyraldehyde
https://huagongshe.com/reaction/1274409
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 4-(7-Chloroquinolin-4-yl)butan-1-ol | HCID 22120667 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(7-Chloroquinolin-4-yl)butyraldehyde | HCID 22120673 | — |
Reaction Steps
Oxalyl chloride (0.42 mL of a 2M solution in dry methylene chloride) was placed in an oven-dried flask, cooled to -78° C. and a solution of 99 mg methylsulfoxide in dry methylene chloride (2 mL) added drop by drop to the oxalyl chloride over 3 minutes and stirred for a further 3 minutes. A solution of 4-(7-chloroquinolin-4-yl)butan-1-ol (100 mg) in dry methylene chloride (1 mL) was added to the reaction flask over approx. 3 minutes followed by anhydrous triethylamine (0.42 mL) and the reaction mixture stirred for another 2.5 hours during which time it was allowed warmed up to room temperature. The reaction was quenched by the addition of saturated brine and then partitioned with methylene chloride. The aqueous layer was discarded and the methylene chloride extract dried over anhydrous sodium sulfate powder, filtered and concentrated in vacuo. The title compound was isolated by flash chromatography on silica gel (ethyl acetate:hexane, 2:1; then ethyl acetate), 57 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06156767 |
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| Source dataset | uspto-grants-2000_12 |
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| ORD ID | ord-cb0d1846999c48b7b3ba7a03c6b96910 |
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| Source note | uspto-grants-2000_12 |
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