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HRID 20910作成日:2026年10月25日

Acetic Acid → 1-(6-Benzyloxycarbonylamino-hexanoyl)-4-oxo-pyrrolidine-3-carboxylic Acid Ethyl Ester

https://huagongshe.com/reaction/20910

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Potassium tert-butoxideHCID 23665647—
反応物3-[(6-Benzyloxycarbonylamino-hexanoyl)-ethoxycarbonylmethyl-amino]-propionic Acid Ethyl EsterHCID 57834643—
溶媒TolueneHCID 1140—
生成物1-(6-Benzyloxycarbonylamino-hexanoyl)-4-oxo-pyrrolidine-3-carboxylic Acid Ethyl EsterHCID 68637397—

反応条件

温度0 °C

反応手順

To a suspension of potassium t-butoxide (7.12 g, 64 mmol) in toluene (150 mL) at 0° C. under nitrogen, was added diester 59 (20 g, 44 mmol) in toluene (25 mL) over a 10 min period. The solution was stirred for 30 min at 0° C. and 5 mL of glacial acetic acid was added, immediately followed by 25 g of NaH2PO4.H2O in 250 mL of ice-cold water. The resultant mixture was extracted with chloroform (3×200 mL), and the combined organic extracts were washed twice with phosphate buffer (2×25 mL, pH=7.0), dried over anhydrous sodium sulfate and evaporated to dryness. The residue was dissolved in toluene (300 mL), cooled to 0° C., and extracted with cold pH 9.5 carbonate buffer (3×150 mL). The aqueous extracts were converted to pH 3 with phosphoric acid, and extracted with chloroform (5×125 mL) which were combined, dried, and evaporated to a afford keto ester 60 (12 g, 45%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745608B2
出典データセットuspto-grants-2010_06
ORD IDord-b52b11e75f354ffb8e94fc7089281b49
出典メモuspto-grants-2010_06