HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908225Generated: October 28, 2026
Dimethyl Sulfoxide → 2-Methyltetrahydrofuran
https://huagongshe.com/reaction/1908225
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 5-Fluoro-2-nitrobenzotrifluoride | HCID 223094 | — |
| Reactant | 7-Azabicyclo[2.2.1]heptane hydrochloride | HCID 16279503 | — |
| Solvent | 2-Methyltetrahydrofuran | HCID 7301 | — |
| Product | 2-Methyltetrahydrofuran | HCID 7301 | 95% |
| Product | 7-[4-Nitro-3-(trifluoromethyl)phenyl]-7-azabicyclo[2.2.1]heptane | HCID 57516843 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08598205B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-db3e5e5d6a8c4e48a742f4edc626a208 |
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| Source note | uspto-grants-2013_12 |
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