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HRID 7234作成日:2026年10月25日

Pyridine → n-Fmoc-o-t-butyl-l-serinyl fluoride

https://huagongshe.com/reaction/7234

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Cyanuric fluorideHCID 12664—
反応物N-(9-Fluorenylmethoxycarbonyl)-O-tert-butylserineHCID 2724633—
溶媒DichloromethaneHCID 6344—
生成物n-Fmoc-o-t-butyl-l-serinyl fluorideHCID 11315144—

反応手順

N-FMOC-O-t-Butyl-L-serine (10 g, 26.07 mmol) (Bachem) was dissolved in dichloromethane (135 mL). Pyridine (2.11 mL, 26.07 mmol) (Aldrich) and cyanuric fluoride (3.52 g, 26.07 mmol) (Aldrich) were successively added at room temperature and the mixture was stirred overnight. Ice cold water (100 mL) was added and the resulting slurry was filtered. The filtrate was poured into a separatory funnel and the layers were separated. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to afford N-FMOC-O-t-butyl-L-serinyl fluoride as a colorless oil which solidified upon standing. (Yield 9.79 g., 97%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084270B2
出典データセットuspto-grants-2006_08
ORD IDord-7e467cb3ee834f5c8c6a348a4e446e43
出典メモuspto-grants-2006_08