HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975474Generated: October 30, 2026
Dimethyl Sulfoxide → HCID 19099323, compound
https://huagongshe.com/reaction/1975474
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 19099247 | HCID 19099247 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19099323 | HCID 19099323 | 9.2% |
Reaction Steps
To a solution of oxalyl chloride (23 ml) in dichloromethane was added dropwise dimethyl sulfoxide (374 ml) while keeping the temperature below -50° C. After the mixture was stirred for 30 minutes at -50° C.~-60° C., 1.2-bis(benzyloxycarbonyl)-4-(1-hydroxyethyl)pyrazolidine (675 g) was added dropwise below -50° C. After the mixture was stirred for 45 minutes at -50° C.~-60° C., triethylamine (122 ml) was added dropwise below -50° C. The reaction mixture was allowed to warm to 0° C. and quenched with water (500 ml). The aqueous layer was separated and extracted twice with dichloromethane (200 ml×2). The combined organic layer was washed with 1N hydrochloric acid (200 ml×2), saturated sodium bicarbonte (200 ml), and 5% sodium chloride (200 ml), dried over magnesium sulfate, and evaporated under reduced pressure. The residue was chromatographed on silica gel (820 ml, hexane:ethyl acetate=2:1~1:1) to give 1,2-bis(benzyloxycarbonyl)pyrazolidin-4-yl methyl ketone (61.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05286721 |
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| Source dataset | uspto-grants-1994_02 |
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| ORD ID | ord-001b5da0991448ed86e080fad5263e4f |
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| Source note | uspto-grants-1994_02 |
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