HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1088280Generated: October 31, 2026
Dimethyl Sulfoxide → HCID 15671519, compound
https://huagongshe.com/reaction/1088280
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 15671483 | HCID 15671483 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15671519 | HCID 15671519 | — |
Reaction Steps
Oxalyl chloride (0.32 ml) was dissolved in 7.9 ml of dry dichloromethane, and 0.56 ml of dry dimethylsulfoxide was added thereto at -45° to -56° C. in a nitrogen stream, followed by stirring at the same temperature for 20 minutes. To the reaction mixture was added a solution of 1.30 g of (2R,4R)-1-benzyloxycarbonyl-2-(3-hydroxypropyl)-4-t-butyldimethylsilyloxypyrrolidine in 6.2 ml of dry dichloromethane at -50° to -60° C., followed by stirring at the same temparature for 15 minutes. Then, 2.2 ml of triethylamine was added thereto at -50° to -60° C. The temparature was elevated to room temperature, and the reaction mixture was washed successively with brine, dilute hydrochloric acid and brine, dried over anhydrous sodium sulfate and distilled to obtain (2R,4R)-1-benzyloxycarbonyl-2-(2-formylethyl)-4-t-butyldimethylsilyloxypyrrolidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04962103 |
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| Source dataset | uspto-grants-1990_10 |
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| ORD ID | ord-92219e2baf2d4962a73a0c6921bca0ed |
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| Source note | uspto-grants-1990_10 |
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