HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1261850Generated: October 30, 2026
Dimethyl Sulfoxide → HCID 86652423, compound
https://huagongshe.com/reaction/1261850
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 67093162 | HCID 67093162 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86652423 | HCID 86652423 | 111.8% |
Reaction Steps
Dimethyl sulfoxide (498 mg, 6.38 mmol) was added at −70° C. to a solution of oxalyl chloride (405 mg, 3.19 mmol) in DCM (5 mL), then after 15 min a solution of (3S,5S)-3-allyl-5-hydroxymethyl-morpholine-4-carboxylic acid tert-butyl ester (547 mg, 2.13 mmol) in DCM (3 mL) was added. The reaction mixture was stirred at −70° C. for 30 min, then treated with Et3N (1.29 g, 12.8 mmol), then after 20 min the ice bath was removed. After 30 min the reaction mixture was washed with sat. aq. sodium hydrogencarbonate solution. The organic layer was washed with brine, dried over magnesium sulfate, filtered, and evaporated to afford the title compound (608 mg) as a light yellow gum, which was directly used in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08471004B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-ba2f7add54cb478692a7d180875a94a1 |
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| Source note | uspto-grants-2013_06 |
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