戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 8726作成日:2026年10月24日

Water → 1,1-Dimethylethyl 3,4-dihydro-5-(hydroxymethyl)-2(1H)-isoquinolinecarboxylate

https://huagongshe.com/ja/reaction/8726

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Ammonium ChlorideHCID 25517—
反応物Sodium borohydrideHCID 4311764—
反応物Tert-butyl 5-formyl-1,2,3,4-tetrahydroisoquinoline-2-carboxylateHCID 22335239—
溶媒MeOH tetrahydrofuranHCID 21899815—
生成物1,1-Dimethylethyl 3,4-dihydro-5-(hydroxymethyl)-2(1H)-isoquinolinecarboxylateHCID 6956121668.8%

反応手順

To solution of 5-formyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester 20a (0.44 g, 1.71 mmol) in 40 mL of methanol:tetrahydrofuran (1:1) at room temperature was added sodium borohydride (0.072 g, 1.88 mmol), and the mixture was stirred to room temperature for 3 h. Water (30 mL) was added followed by ammonium chloride saturated solution (20 mL) and the product was extracted with dichloromethane. The combined organics were dried over magnesium sulfate, the solvent was evaporated and the residue was purified by flash chromatography eluting with 30% ethyl acetate in hexanes, to yield 0.31 g of 5-hydroxymethyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester 21a.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091200B2
出典データセットuspto-grants-2006_08
ORD IDord-b8ea807d82c04522b1c9cb4cd3a35d20
出典メモuspto-grants-2006_08