HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534083Generated: October 30, 2026
Dimethyl Sulfoxide → HCID 86644155, compound
https://huagongshe.com/reaction/534083
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 67486253 | HCID 67486253 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Chlorine | HCID 24526 | — |
| Product | HCID 86644155 | HCID 86644155 | 110.4% |
Reaction Steps
A solution of methylsulfinylmethane (20.6 ml, 289 mmol) in CH2 Cl2 (260 mL) at −60° C., was added dropwise to a 2M solution of oxalyl dichloride (15.2 ml, 174 mmol) in CH2Cl2 (80 mL). The mixture was stirred for 20 minutes and then a solution of ((2S,3S)-3-(methoxymethyl)-1,4-dioxaspiro[4.5]decane-2-yl)methanol (31.3 g, 145 mmol) in CH2Cl2 (80 mL) was added dropwise. The mixture was stirred for 10 minutes and then triethylamine (101 ml, 724 mmol) was slowly added. The reaction mixture was warmed to ambient temperature and water was added. When the mixture became clear, it was extracted with CH2Cl2, dried over sodium sulfate, filtered and concentrated to afford crude ((2R,3S)-3-(methoxymethyl)-1,4-dioxaspiro[4.5]decane-2-carbaldehyde (34.3 g, 96.2% yield, 87% pure) which was taken on to next reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853409B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-3dccb769a1674022b867e491cacdae67 |
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| Source note | uspto-grants-2014_10 |
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