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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908225Generated: October 28, 2026

Dimethyl Sulfoxide → 2-Methyltetrahydrofuran

https://huagongshe.com/reaction/1908225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantSodium CarbonateHCID 10340—
Reactant5-Fluoro-2-nitrobenzotrifluorideHCID 223094—
Reactant7-Azabicyclo[2.2.1]heptane hydrochlorideHCID 16279503—
Solvent2-MethyltetrahydrofuranHCID 7301—
Product2-MethyltetrahydrofuranHCID 730195%
Product7-[4-Nitro-3-(trifluoromethyl)phenyl]-7-azabicyclo[2.2.1]heptaneHCID 57516843—

Reaction Conditions

Temperature55 °C

Reaction Steps

4-fluoro-1-nitro-2-(trifluoromethyl)benzene (18) (901 g) was added into a 30 L jacketed vessel. Sodium carbonate (959.1 g) and 5 L dimethylsulfoxide (DMSO) was added and the mixture was stirred under a nitrogen atmosphere. 7-azabicyclo[2.2.1]heptane hydrochloride (7a) (633.4 g) was added to the vessel in portions. The temperature of the mixture was gradually raised to 55° C., and the reaction was monitored by HPLC. When the substrate was less than 1% AUC, the reaction was considered complete. The mixture was then diluted with 10 vol. 2-methyltetrahydrofuran and washed with 5.5 vol. water three times until no DMSO remained in the aqueous layer as determined by HPLC, to give 7-[4-nitro-3-(trifluoromethyl) phenyl]-7-azabicyclo[2.2.1]heptane (19) in 2-methyltetrahydrofuran (approximately 95% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598205B2
Source datasetuspto-grants-2013_12
ORD IDord-db3e5e5d6a8c4e48a742f4edc626a208
Source noteuspto-grants-2013_12