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HRID 719110作成日:2026年10月26日

Ninhydrin → Methyl (R)-2-Amino-3-(trimethylsilyl)propanoate

https://huagongshe.com/reaction/719110

反応式

関与物質

役割名称HCID仕込み量
反応物NinhydrinHCID 10236—
反応物Sodium CarbonateHCID 10340—
反応物(2R)-2-amino-3-(trimethylsilyl)propanoic acidHCID 11008231—
反応物Boron, trifluoro(methanol)-, (T-4)-HCID 11062313—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
溶媒Dichloromethane methanolHCID 21226129—
生成物Methyl (R)-2-Amino-3-(trimethylsilyl)propanoateHCID 5930239792%

反応条件

温度70 °C

反応手順

3-Trimethylsilyl alanine (J. Organomet. Chem., 628, (2001), 183–194; 19 mg, 0.118 mmol) was mixed with 3 ml BF3-MeOH (14%, 3.7 mmol) in a sealed tube and heated to 70° C. Analysis was performed using TLC (MeOH:DCM 1:9, stained w. ninhydrine in ethanol). The mixture was heated for 3 h and was then cooled to ambient temperature. The mixture was poured into a mixture of 3 ml EtOAc and 2 ml water containing Na2CO3. More Na2CO3 (5%-aq) was added until pH ca 7. The aqueous phase was washed with EtOAc (2×3 ml). The combined organic layers were washed with brine (1 ml), dried with Na2SO4 and evaporated. The product was obtained as a white film. Mass: 19 mg (92% yield). NMR (CDCl3): 0.1 (s, 9H), 1.2–1.4 (m, 2H), 3.8 (s, 3H), 4.2 (brs, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07132416B2
出典データセットuspto-grants-2006_11
ORD IDord-5929ac61b44f44a68d65dad6554dcc85
出典メモuspto-grants-2006_11