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HRID 2199473作成日:2026年10月26日

Cyclohexane → HCID 86730041、化合物

https://huagongshe.com/reaction/2199473

反応式

関与物質

役割名称HCID仕込み量
反応物CyclohexaneHCID 8078—
反応物Sodium BicarbonateHCID 516892—
反応物(S)-(-)-1-Amino-2-(methoxymethyl)pyrrolidineHCID 7156993—
反応物6-iodo-3,4-dihydronaphthalen-1(2H)-oneHCID 45489800—
触媒p-Toluenesulfonic acid monohydrateHCID 521998—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物HCID 86730041HCID 8673004198.7%

反応手順

To a stirred mixture of 6-iodo-3,4-dihydronaphthalen-1(2H)-one (I-8A, 20.90 g, 77 mmol), p-toluenesulfonic acid monohydrate (0.584 g, 3.07 mmol), and cyclohexane (40 mL) was added (S)-2-(methoxymethyl)pyrrolidin-1-amine (10 g, 77 mmol) dropwise at room temperature under nitrogen. The mixture was heated with azeotropic removal of water for 5 h. The reaction mixture was diluted with ethyl acetate (20 mL) and mixed with saturated aqueous sodium bicarbonate solution (15 mL). The aqueous layer was separated and extracted with ethyl acetate (2×30 mL). The combined organic solutions were dried over anhydrous sodium sulfate and concentrated under reduced pressure. Flash chromatography purification (330 g silica gel column, gradient elution from 0% to 20% EtOAc in hexanes) afforded (S)—N-(6-iodo-3,4-dihydronaphthalen-1(2H)-ylidene)-2-(methoxymethyl)pyrrolidin-1-amine (29.1 g, 76 mmol) as a yellow liquid. LC/MS M+1=385.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09359286B2
出典データセットuspto-grants-2016_06
ORD IDord-1445f10207fe4433a9bd0f756acc0296
出典メモuspto-grants-2016_06