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HRID 444993作成日:2026年10月26日

Nitrogen → 2-[10-(4-tert-Butoxycarbonylphenoxy)decanoylamino]pentanedioic acid 5-benzyl ester 1-tert-butyl ester

https://huagongshe.com/reaction/444993

反応式

関与物質

役割名称HCID仕込み量
反応物NitrogenHCID 947—
反応物Potassium CarbonateHCID 11430—
反応物tert-Butyl 4-hydroxybenzoateHCID 117640—
反応物2-(10-Bromodecanoylamino)pentanedioic acid 5-benzyl ester 1-tert-butyl esterHCID 59687918—
溶媒AcetonitrileHCID 6342—
生成物2-[10-(4-tert-Butoxycarbonylphenoxy)decanoylamino]pentanedioic acid 5-benzyl ester 1-tert-butyl esterHCID 59687925110.6%

反応手順

4-Hydroxy-benzoic acid tert-butyl ester (0.65 g, 3.08 mmol) was dissolved in acetonitrile (7.5 ml) and added to 2-(10-Bromodecanoylamino) pentanedioic acid 5-benzyl ester 1-tert-butyl ester (1.62 g, 3.08 mmol). Acetonitrile (90 ml) and K2CO3 (0.64 g, 4.62 mmol) was added and the mixture was refluxed for 16 h under a flow of N2. The solvent was removed under vacuum. AcOEt (100 ml) was added and the solution was washed with water (2×50 ml) using sat. NaCl and methanol to aid phase separation, dried over MgSO4, and concentrated to yield a light brown oil (2.18 g). The oil was purified by flash chromatography (silica, 95:5 DCM/AcOEt) to yield an oil (160 mg, 8%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08476228B2
出典データセットuspto-grants-2013_07
ORD IDord-685280ad0fbc4fcb9cd4dec5394b55cc
出典メモuspto-grants-2013_07