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HRID 1454214作成日:2026年10月27日

Acetic Acid → HCID 178525439、化合物

https://huagongshe.com/reaction/1454214

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物6-Aminohexanoic AcidHCID 564—
反応物Sodium borohydrideHCID 4311764—
反応物FerrocenecarboxyaldehydeHCID 15184314—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒Sodium HydroxideHCID 14798—
生成物HCID 178525439HCID 178525439—

反応条件

温度80 °C

反応手順

After 1.38 g (6.4 mmol) of ferrocene-aldehyde (Aldrich Corp) was dissolved in 20 mL of a DMF solution, the mixture was mixed with a solution of 0.75 g (5.7 mmol) of 6-amino caproic acid (Merck Corp.) in 5 mL of NaOH and refluxed at 80° C. for 2 hours. The reaction mixture was cooled to room temperature, and a solution of NaBH4 (0.63 g, 16.5 mmol) in 5 mL of water was added little by little into the reaction mixture (refer to FIG. 11). After 12 hours later, an aqueous acetic acid solution (10%) was slowly added until the pH reached 5. The reaction by-product ferrocene-CH2OH and unreacted 6-amino caproic acid dissolved in the organic phase was removed through extraction using ethylacetate. The aqueous phase was distilled at 50° C. under reduced pressure to obtain yellowish brown crystals. The yellowish brown crystals were recrystallized by dissolving the crystals in high-temperature ethanol to obtain planar, yellow crystalline N-(ferrocenyl methyl)-6-amino caproic acid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07479254B2
出典データセットuspto-grants-2009_01
ORD IDord-c2e5a198e4eb4adda1d5c178e958d27f
出典メモuspto-grants-2009_01