HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1919096Generated: November 2, 2026
Sodium bis(trimethylsilyl)amide → tert-Butyl 3-(4-aminophenyl)azetidine-1-carboxylate
https://huagongshe.com/reaction/1919096
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | 4-Aminophenylboronic acid | HCID 2734615 | — |
| Reactant | cis-2-Aminocyclohexanol | HCID 6542151 | — |
| Reactant | Tert-butyl 3-iodoazetidine-1-carboxylate | HCID 11000522 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | tert-Butyl 3-(4-aminophenyl)azetidine-1-carboxylate | HCID 56956222 | 41.1% |
Reaction Steps
A mixture of tert-butyl 3-iodoazetidine-1-carboxylate (1 g, 3.53 mmol), 4-aminophenylboronic acid (630 mg, 4.59 mmol), NiI2 (66 mg, 0.212 mmol), NaHMDS (1.94 g, 10.6 mmol), (1R,2S)-2-aminocyclohexanol (24 mg, 0.212 mmol) in isopropanol (8 mL) was stirred at 150° C. in microwave for 2 h. It was then evaporated and the residue was dissolved with water and ethyl acetate. The water phase was separated and extracted with ethyl acetate. The combined extracts were dried over sodium sulfate and concentrated under reduced pressure. The residue was purified with column chromatography to give 298a (360 mg, 40%). MS: [M+H]+ 249.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08618107B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-e09953a953564a3fb1a163176382d031 |
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| Source note | uspto-grants-2013_12 |
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