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HRID 529366作成日:2026年10月25日

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

https://huagongshe.com/reaction/529366

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium Phosphate, TribasicHCID 62657—
反応物TricyclohexylphosphineHCID 75806—
反応物Cyclopropylboronic acidHCID 2760897—
反応物tert-butyl ((1R,2S)-2-(4-bromophenyl)cyclopropyl)carbamateHCID 86658779—
触媒palladium(II) acetateHCID 167845—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物tert-Butyl ((trans)-2-(4-cyclopropylphenyl)cyclopropyl)carbamateHCID 8670826576.2%

反応条件

温度100 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09346840B2
出典データセットuspto-grants-2016_05
ORD IDord-9c3fafdd5ae248e489e94b595a8c45a4
出典メモuspto-grants-2016_05