Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant4-Aminophenylboronic acidHCID 2734615—
Reactantcis-2-AminocyclohexanolHCID 6542151—
ReactantTert-butyl 3-iodoazetidine-1-carboxylateHCID 11000522—
SolventIsopropanolHCID 3776—
Producttert-Butyl 3-(4-aminophenyl)azetidine-1-carboxylateHCID 5695622241.1%

Reaction Conditions

Temperature150 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618107B2
Source datasetuspto-grants-2013_12
ORD IDord-e09953a953564a3fb1a163176382d031
Source noteuspto-grants-2013_12