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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 529366Erstellt: 25. Oktober 2026

Potassium Phosphate, Tribasic → tert-Butyl ((trans)-2-(4-cyclopropylphenyl)cyclopropyl)carbamate

https://huagongshe.com/reaction/529366

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium Phosphate, TribasicHCID 62657—
EduktTricyclohexylphosphineHCID 75806—
EduktCyclopropylboronic acidHCID 2760897—
Edukttert-butyl ((1R,2S)-2-(4-bromophenyl)cyclopropyl)carbamateHCID 86658779—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
Produkttert-Butyl ((trans)-2-(4-cyclopropylphenyl)cyclopropyl)carbamateHCID 8670826576,2%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a 30-mL microwave tube were added tert-butyl (trans-2-(4-bromophenyl)cyclopropyl)carbamate (400 mg, 1.281 mmol), cyclopropylboronic acid (143 mg, 1.666 mmol), potassium phosphate (952 mg, 4.48 mmol), tricyclohexylphosphine (35.9 mg, 0.128 mmol), toluene (4 mL) and water (0.2 mL), and the mixture was degassed by bubbling N2. Palladium(II) acetate (14.38 mg, 0.064 mmol) was added and the tube was sealed. The mixture was heated at 100° C. with stirring for 4 h. The mixture was cooled and quenched with water (5 mL) and extracted with EtOAc (3×). The extract was dried (Na2SO4) and concentrated. The residue was purified using column chromatography (silica gel, 0 to 70% EtOAc/hexanes) to give 267 mg of product as pale yellow solid. MS: (M+H)+=274.2. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 0.61-0.73 (m, 2H), 0.90-1.01 (m, 2H), 1.08-1.24 (m, 2H), 1.42-1.52 (s, 9H), 1.81-1.94 (m, 1H), 1.98-2.12 (m, 1H), 2.70 (br. s., 1H), 6.91-7.12 (m, 4H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09346840B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-9c3fafdd5ae248e489e94b595a8c45a4
Quellennotizuspto-grants-2016_05