HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359361Generated: November 2, 2026
Dimethyl Sulfoxide → HCID 70145969, compound
https://huagongshe.com/reaction/2359361
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Tert-butyl 3-aminoazetidine-1-carboxylate | HCID 1516507 | — |
| Reactant | 5-Fluoro-2-nitroanisole | HCID 2779250 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 70145969 | HCID 70145969 | 116.6% |
Reaction Steps
Into a 100 mL 3-Neck round-bottomed flask equipped with reflux condenser were charged 4-fluoro-2-methoxy-1-nitrobenzene (4.086 g) and tert-butyl 3-aminoazetidine-1-carboxylate (4.4 g), triethylamine (9.6 mL), and dimethyl sulfoxide (20 mL). The reaction mixture was heated at 95° C. for 8 hours. The reaction mixture was poured into water (200 mL) and extracted with ethyl acetate (50 mL×3). The organic layer was washed with brine (50 mL×2), dried over sodium sulfate, and concentrated completely under reduced pressure at 40° C. to give the title compound (9 g) which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08685988B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-eccb53e07b0a48df83f8ca257b0fc30d |
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| Source note | uspto-grants-2014_04 |
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