HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710791Generated: November 3, 2026
Dimethyl Sulfoxide → HCID 59457459, compound
https://huagongshe.com/reaction/1710791
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Trimethylamine oxide | HCID 1145 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | HCID 59457464 | HCID 59457464 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 59457459 | HCID 59457459 | 41% |
Reaction Steps
A cold (−20° C.) solution of anhydrous trimethylamine N-oxide (2.10 g, 27.96 mmol) in a dry mixture of dichloromethane and dimethylsulfoxide (20 ml, 1/3 v/v) is treated with a solution of 4-chloromethyl-2-[4-(3-chloro-propoxy)-phenyl]-oxazole ax57 (2.00 g, 6.99 mmol) in the same mixture of solvents (20 ml). The mixture is then allowed to warm up to 20° C. and is stirred at that temperature for 24 h. The dark mixture is then poured into water (50 ml) and extracted with dichloromethane. The organic phases are concentrated and the resulting DMSO solution is treated with ether and water. The heterogeneous mixture is further extracted with ether (2×20 ml). The organic phases are then dried over magnesium sulfate and concentrated to afford 760 mg of 2-[4-(3-chloro-propoxy)-phenyl]-oxazole-4-carbaldehyde i100.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07790720B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-2fcc531f785c4f0685fbc1d85a92203f |
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| Source note | uspto-grants-2010_09 |
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