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HRID 2183532作成日:2026年10月27日

Chlorotrimethylsilane → (2S)-2-acetamido-3-(4-iodophenyl)propanoic acid

https://huagongshe.com/reaction/2183532

反応式

関与物質

役割名称HCID仕込み量
反応物ChlorotrimethylsilaneHCID 6397—
反応物Acetic AnhydrideHCID 7918—
反応物TriethylamineHCID 8471—
反応物2-Amino-3-(4-iodophenyl)propionic acidHCID 5152312—
溶媒DichloromethaneHCID 6344—
生成物(2S)-2-acetamido-3-(4-iodophenyl)propanoic acidHCID 6862488695%

反応条件

温度0 °C

反応手順

A solution of 15 g (51 mmol) of 4-iodo-D,L-phenylalanine and 16.2 ml (127.5 mmol) of Me3SiCl in 150 mL of dichloromethane was heated at reflux for 1 h under N2. The reaction mixture was cooled to 0° C. with an ice bath and 17.7 mL (127 mmol) of triethyl amine was added, followed by 5.83 mL (61.2 mmol) of acetic anhydride. The mixture was stirred at 0° C. for 30 min, then warmed up to room temperature and stirred for another 30 min. The reaction was quenched by adding 1M aqueous sodium hydroxide and then the mixture was acidified with 2M aqueous hydrogen chloride to pH 1. The precipitate was collected by filtration and dried under vacuum to afford 16 g (95%) of N-acetyl-4-iodophenylalanine as a white solid: 1H NMR (DMSO-d6) 8.19 (d, 1H), 7.61 (d, 2H), 7.02 (d, 2H), 4.39-4.31 (m, 1H), 3.01-2.92 (dd, 1H), 3.80-2.69 (dd, 1H), 2.67 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06900213B2
出典データセットuspto-grants-2005_05
ORD IDord-e1426e67f5c2421a9645546d0ccdc35e
出典メモuspto-grants-2005_05