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HRID 25660作成日:2026年10月25日

Acetic Acid → 5-[4-(tert-Butoxycarbonyl-methyl-amino)-cyclohexylidene]-pentanoic acid

https://huagongshe.com/reaction/25660

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Sodium hydrideHCID 24758—
反応物(4-Carboxybutyl)triphenylphosphonium bromideHCID 161236—
反応物tert-butyl N-methyl-N-(4-oxocyclohexyl)carbamateHCID 24820328—
溶媒DimethylformamideHCID 6228—
生成物5-[4-(tert-Butoxycarbonyl-methyl-amino)-cyclohexylidene]-pentanoic acidHCID 2256768285.6%

反応手順

5 g (21.99 mmol) Methyl-(4-oxo-cyclohexyl)-carbamic acid tert-butyl ester and 12.68 g (28.59 mmol) (4-Carboxy-butyl)-triphenyl-phosphonium bromide were dispended in 50 ml DMF. In small portions 2.49 g (57.2 mmol, 55%) NaH were added and the slurry was diluted by adding 50 ml DMF. The mixture was stirred at RT over night, 10 ml AcOH were added and the solvent was evaporated under reduced pressure. The residue was dissolved in ether and water, and the inorganic layer was extracted with ether. The combined organic phases were dried over and the crude materil was purified by column chromatography with ETOAc/hexane to give 5.86 g (83%)5-[4-(tert-Butoxycarbonyl-methyl-amino)-cyclohexylidene]-pentanoic acid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06858651B2
出典データセットuspto-grants-2005_02
ORD IDord-6ed6edff7c4840dc8c5284f235649c74
出典メモuspto-grants-2005_02