HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050894Generated: October 31, 2026
Dimethyl Sulfoxide → HCID 86744770, compound
https://huagongshe.com/reaction/2050894
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 1-Azabicyclo(2.2.2)octane-4-methanol | HCID 141311 | — |
| Reactant | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 86744770 | HCID 86744770 | — |
Reaction Steps
1.6 cm3 of dimethyl sulfoxyde are added dropwise to a mixture, cooled to -50°/-60° C., of 1.09 cm3 of oxalyl chloride and 30 cm3 of methylene chloride, after agitating for 15 minutes, 1.6 g of 4-hydroxy methylquinuclidine (Helv. Chim. Acta 57 (8) 2332 (1974)) in 50 cm3 of methylene chloride are added and the medium is agitated for 2 hours at -50°/-60° C. Then, 7.89 cm3 of triethylamine are added dropwise. The mixture is allowed to warm at room temperature, a solution of 0.95 g of O-methyl hydroxylamine hydrochloride in 30 cm3 of methanol is added and the reaction medium is maintained for 16 hours to room temperature. The solvents are evaporated to dryness, the residue is taken up with dichloromethane, alkalized with 2N sodium hydroxyde, after decantation the aqueous phase is then extracted with dichloromethane. The organic extracts are evaporated to dryness. The residue is dissolved in ethyl ether and the hydrochloride is obtained using gaseous hydrochloric acid. The solid is filtered off and crystallised in a mixture of ethanolethyl ether. 0.91 g of expected product is obtained. M.P.=271°-271.5° C. (with decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05015655 |
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| Source dataset | uspto-grants-1991_05 |
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| ORD ID | ord-a2fc843d51374b61ab5ad40e611e1fb5 |
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| Source note | uspto-grants-1991_05 |
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