HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550233Generated: October 29, 2026
Dimethyl Sulfoxide → 4-Bromonaphthalene-2-carbaldehyde
https://huagongshe.com/reaction/550233
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 21906498 | HCID 21906498 | — |
| Reactant | 874357-17-2 | HCID 59869315 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Bromonaphthalene-2-carbaldehyde | HCID 54338128 | 78% |
Reaction Steps
Under a nitrogen atmosphere, an oxalyl chloride methylene chloride solution (2.0 M, 4.88 ml) was diluted with methylene chloride (40 ml), and dimethyl sulfoxide (0.9 ml, 12.7 mmol) was added dropwise thereto at −78° C. To this solution, a solution of (4-bromonaphthalene-2-yl)-methanol (1.15 g, 4.88 mmol) as synthesized according to a document [J. Med. Chem., 37, 2485 (1993)] in methylene chloride (10 ml) was added dropwise over 10 minutes. This reaction mixture was stirred at −78° C. for 15 minutes and −45° C. for one hour, and then triethylamine (4.0 ml, 29.3 mmol) was added dropwise thereto and stirred at 0° C. for 30 minutes. To the reaction solution, a saturated ammonium chloride aqueous solution was added and the resulting solution was extracted with methylene chloride. The organic layer was washed with water and a saturated sodium chloride aqueous solution, and dried with sodium sulfate. After filtration, the solvent was distilled under reduced pressure, and the obtained residue was purified by silica gel column chromatography [developing solution=ethyl acetate:n-hexane (1:20)] to obtain the title compound (890 mg, 78%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07943748B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-18e6034387304741bbd97e86c968b6a2 |
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| Source note | uspto-grants-2011_05 |
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