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HRID 61427作成日:2026年10月26日

Acetic acid, 2-(triphenylphosphoranylidene)-, methyl ester → 1,2-dibenzyl 3-tert-butyl (2S,3S)-5-(2-methoxy-2-oxoethylidene)piperidine-1,2,3-tricarboxylate

https://huagongshe.com/reaction/61427

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic acid, 2-(triphenylphosphoranylidene)-, methyl esterHCID 17453—
反応物1,2-Dibenzyl 3-(tert-butyl) (2S,3S)-5-oxopiperidine-1,2,3-tricarboxylateHCID 59305104—
溶媒TolueneHCID 1140—
生成物1,2-dibenzyl 3-tert-butyl (2S,3S)-5-(2-methoxy-2-oxoethylidene)piperidine-1,2,3-tricarboxylateHCID 8662148680%

反応手順

To an oven-dried 25 mL round-bottomed flask equipped with a magnetic stir bar and under a nitrogen gas atmosphere was placed methyl(triphenylphosphoranylidene)acetate (199 mg, 0.597 mmol) and toluene (5 mL). To this heterogeneous solution was added a solution of 1,2-dibenzyl 3-tert-butyl(2S,3S)-5-oxopiperidine-1,2,3-tricarboxylate (93 mg, 0.199 mmol) in toluene (3 mL). The reaction mixture was heated to reflux and stirred overnight. The volatiles were then removed in-vacuo and the yellow oil was purified by Combiflash (10 to 30% ethyl acetate in hexanes) to afford 83 mg (80%) of 1,2-dibenzyl 3-tert-butyl(2S,3S)-5-(2-methoxy-2-oxoethylidene)piperidine-1,2,3-tricarboxylate. LCMS (ESI): 424 (M-CO2t-Bu+2H+), 468 (M-t-Bu+2H+), 524 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09440958B2
出典データセットuspto-grants-2016_09
ORD IDord-bae75d4a6891464a8177acd553e9ae94
出典メモuspto-grants-2016_09