戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 236337作成日:2026年10月24日

Methanol → methyl (3S)-1,2,3,4-tetrahydroisoquinoline-3-carboxylate hydrochloride

https://huagongshe.com/ja/reaction/236337

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Thionyl ChlorideHCID 24386—
反応物1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acidHCID 95489—
生成物methyl (3S)-1,2,3,4-tetrahydroisoquinoline-3-carboxylate hydrochlorideHCID 2760578—

反応手順

In succession 5 g of tetrahydroisoquinoline 3-carboxylic acid and 30 ml of methanol are introduced into a three-necked flask. 6 g of thionyl chloride are added to this suspension by pouring carefully, taking care that the temperature does not exceed 0, +5°. The addition takes approximately 10 minutes. After the addition is completed, stirring is continued for 2 hours at room temperature, and then the mixture is heated to reflux for 11/2 hours. Once the mixture has dissolved completely, heating is discontinued and the mixture is then evaporated to dryness. The residue is taken up three times in methanol and then evaporated to dryness. Finally, 8 g of colourless crystals are obtained and purified by trituration with ether. The crystals are separated off by filtration, washed with ether and dried. 6.4 g of methyl tetrahydroisoquinoline-3-carboxylate hydrochloride are thus obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04644008
出典データセットuspto-grants-1987_02
ORD IDord-f6519eaa5551445a8f560472842abe6d
出典メモuspto-grants-1987_02