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HRID 1171855作成日:2026年10月25日

Toluene → (S)-1-phenyl-1,2,3,4-tetrahydroisoquinoline-2-carboxylic acid 2-methylpropan-2-yl ester

https://huagongshe.com/reaction/1171855

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Potassium CarbonateHCID 11430—
反応物(1S)-1,2,3,4-Tetrahydro-1-phenylisoquinolineHCID 1382087—
反応物Tert-butyldicarbonateHCID 22064466—
溶媒WaterHCID 962—
生成物(S)-1-phenyl-1,2,3,4-tetrahydroisoquinoline-2-carboxylic acid 2-methylpropan-2-yl esterHCID 67079183—

反応条件

温度20 °C

反応手順

A 10.00 g portion of (S)-1-phenyl-1,2,3,4-tetrahydroisoquinoline and 10.41 g of tert-butyl dicarbonate were added to a mixture of 50 ml of toluene, 6.95 g of potassium carbonate and 30 ml of water and stirred at 20° C. overnight, and then the organic layer was washed with 30 ml of water. The thus obtained organic layer was concentrated under a reduced pressure and then dried to obtain 14.59 g of (S)-1-phenyl-1,2,3,4-tetrahydroisoquinoline-2-carboxylic acid 2-methylpropan-2-yl ester (1H-NMR (DMSO-d6, tetramethylsilane internal standard, 80° C.): δ 1.39 (9H, s), 2.72-2.91 (2H, m), 3.28-3.32 (1H, m), 3.80-3.89 (1H, m), 6.18 (1H, s), 7.07-7.33 (9H, m), mass spectrum: m/z=310 [M +H]+ (FAB)).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07829715B2
出典データセットuspto-grants-2010_11
ORD IDord-597f24066c024dbba993abfd61a7a4d4
出典メモuspto-grants-2010_11