Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2081243Generated: November 4, 2026

Dimethyl Sulfoxide → HCID 86744770, compound

https://huagongshe.com/reaction/2081243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantOxalyl chlorideHCID 65578—
Reactant1-Azabicyclo(2.2.2)octane-4-methanolHCID 141311—
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 86744770HCID 86744770—

Reaction Conditions

Temperature-60 °C

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 crystallized in a mixture of ethanol-ethyl ether. 0.91 g of expected product is obtained. M.P.=271°-271,5° C. (with decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05183893
Source datasetuspto-grants-1993_02
ORD IDord-5e9f94a661ff4198a3f1f59fc6f8423f
Source noteuspto-grants-1993_02