HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604339Generated: October 29, 2026
Dimethyl Sulfoxide → HCID 67065856, compound
https://huagongshe.com/reaction/604339
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 58455161 | HCID 58455161 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67065856 | HCID 67065856 | — |
Reaction Steps
To a stirred solution of anhydrous dichloromethane (35.0 mL) in a 3-necked flask with a thermometer, oxalyl chloride (1.5 mL) was added and the resulting solution was cooled to −60° C. A solution of dimethylsulfoxide (2.6 mL) in dichloromethane (7.5 mL) was added over a period of 10 min, and then (3R)-1-tritylpyrrolidin-3-ol (5.0 g) in dichloromethane (15.0 mL) was added over a period of 10 min. The resulting solution was stirred at −60° C. for 15 min, then triethylamine (10.6 mL) was added over a period of 5 min. After 5 min, the cooling bath was removed and the mixture was allowed to warm to room temperature. Water (45 mL) was added. The mixture was stirred for an additional 30 min and then extracted with dichloromethane. The organic phase was washed with 5% aqueous citric acid solution, dried over anhydrous sodium sulfate, filtered and concentrated to yield the title compound. LC-MS=243.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07910596B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-e36450ee9c404cef81211f4b6bc6f4e2 |
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| Source note | uspto-grants-2011_03 |
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