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HRID 428320作成日:2026年10月25日

Vinyl isobutyl ether → HCID 54165959、化合物

https://huagongshe.com/reaction/428320

反応式

関与物質

役割名称HCID仕込み量
反応物Vinyl isobutyl etherHCID 7992—
反応物TriethylamineHCID 8471—
反応物1,3-Bis(diphenylphosphino)propaneHCID 81219—
反応物(R)-3-(2-benzyloxy)-5-bromophenyl)-N,N-diisopropyl-3-phenylpropan-1-amineHCID 24885301—
触媒palladium(II) acetateHCID 167845—
溶媒DimethylformamideHCID 6228—
生成物HCID 54165959HCID 54165959—

反応条件

温度100 °C

反応手順

To a stirred solution of (R)-N,N-diisopropyl-3-(2-benzyloxy-5-bromophenyl)-3-phenylpropanamine (Example 12) (10.2 g, 21.23 mmol) in DMF (100 mL) under nitrogen atmosphere at room temperature were sequentially added triethylamine (2.58 g, 25.47 mmol), TlOAc (6.15 g, 23.35 mmol), isobutylvinylether (14 mL, 106.14 mmol), DPPP (0.87 g, 2.12 mmol) and Pd(OAc)2 (0.24 g, 1.06 mmol). The reaction temperature was raised to 100° C. and stirred for 3 hours, cooled to room temperature, filtered and treated with HCl (5%, 250 mL) and stirred for another 2 hours. The reaction mixture was repeatedly extracted with dichloromethane and the combined organic layers were dried (MgSO4), filtered and the solvent evaporated. Triethylamine and DMF were destined off under reduced pressure to yield 9 g (98%); 1H NMR (CDCl3) δ1.22 (m, 12H), 2.52-2.70 (m, 7H), 3.40 (br, 2H), 4.34 (t, 1H), 5.10 (s, 1H), 6.90 (d, 1H), 7.17-7.40 (m, 10H), 7.82 (m, 1H) and 7.92 (s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06313132B1
出典データセットuspto-grants-2001_11
ORD IDord-1c4499c960ae4932a4e9ac8d078bc00c
出典メモuspto-grants-2001_11