HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303683Generated: November 1, 2026
Dimethyl Sulfoxide → (+)-trans-3-Formyl-4-phenylcyclopentan-1-one
https://huagongshe.com/reaction/2303683
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (+)-trans-3-Hydroxymethyl-4-phenylcyclopentan-1-one | HCID 53754795 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (+)-trans-3-Formyl-4-phenylcyclopentan-1-one | HCID 54453591 | — |
Reaction Steps
To a solution of oxalyl chloride (0.352 mL, 0.512 g, 4.03 mmol) in methylene chloride (8 mL) at −70° C. was added dropwise DMSO (0.573 mL, 0.630 g, 8.06 mmol). After 10 min, a solution of (+)-trans-3-hydroxymethyl-4-phenylcyclopentan-1-one from Example 11, Step F (0.153 g, 0.807 mmol) in methylene chloride (1 mL) was added dropwise. The reaction mixture was stirred at −70° C. for 45 min and then diisopropylethylamine (2.1 mL, 1.6 g, 4.48 mmol) was added. The reaction mixture was allowed to warm to rt for 10 min and then diluted with methylene chloride, poured into water, and extracted three times with methylene chloride. The organic layers were combined, washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo. The crude title compound (0.15 g) was used directly in Step B.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06432981B1 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-81240fd29b0644689b861ae0c90fcb60 |
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| Source note | uspto-grants-2002_08 |
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