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HRID 485741作成日:2026年10月25日

Thionyl Chloride → Chloride

https://huagongshe.com/reaction/485741

反応式

関与物質

役割名称HCID仕込み量
反応物Thionyl ChlorideHCID 24386—
反応物1-Oxo-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acidHCID 4836159—
反応物3-Acetylthiopropionyl chlorideHCID 20041315—
反応物HCID 178467872HCID 178467872—
溶媒BenzeneHCID 241—
溶媒AcetonitrileHCID 6342—
溶媒TriethylamineHCID 8471—
生成物ChlorideHCID 312—
生成物2-(3-Acetylthiopropionyl)-1-oxo-1,2,3,4-tetrahydro-3-isoquinoline carboxylic acidHCID 20269554—

反応手順

1.1 g of triethyl amine was added to a suspension of 1.0 g of 1-oxo-1,2,3,4-tetrahydro-3-isoquinoline carboxylic acid in 10 ml of acetonitrile. A solution of 3-acetylthiopropionyl chloride (3-acethylthiopropionyl chloride was prepared by adding 1.0 g of thionyl chloride to a solution of 0.8 g of 3-acetylthiopropionic acid in 5 ml of benzene, stirring the solution overnight at room temperature and distilling off the solvent and excess thionyl chloride) in 5 ml of acetonitrile was added drop by drop to the suspension which was ice-cooled. After stirring the mixture for 2 hours at room temperature, the solvent was distilled off, 20 ml of ethylacetate and 10 ml of water were added to the residue and the solution was shaken and the organic phase separated and washed. The organic phase was dried over anhydrous Glauber's salt, the solvent was distilled off and then the residue was recrystalized from benzene to obtain 0.9 g of 2-(3-acetylthiopropionyl)-1-oxo-1,2,3,4-tetrahydro- 3-isoquinoline carboxylic acid as a colorless microcrystalline material.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04537967
出典データセットuspto-grants-1985_08
ORD IDord-6a14680f731b4f569539a16a622d5776
出典メモuspto-grants-1985_08