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HRID 2251758作成日:2026年10月26日

5-Hexenal → (R)-3-Hydroxy-1-((R)-4-isopropyl-2-thioxothiazolidin-3-yl)oct-7-en-1-one

https://huagongshe.com/reaction/2251758

反応式

関与物質

役割名称HCID仕込み量
反応物5-HexenalHCID 69817—
反応物DiisopropylethylamineHCID 81531—
反応物(R)-1-(4-isopropyl-2-thioxothiazolidin-3-yl)ethanoneHCID 11745744—
触媒Titanium TetrachlorideHCID 24193—
溶媒DichloromethaneHCID 6344—
生成物(R)-3-Hydroxy-1-((R)-4-isopropyl-2-thioxothiazolidin-3-yl)oct-7-en-1-oneHCID 5964406474%

反応手順

A solution of (R)-1-(4-isopropyl-2-thioxothiazolidin-3-yl)ethanone (11.8 g, 58.1 mmol) in dichloromethane (380 mL) under an atmosphere of nitrogen was cooled to −78° C., titanium tetrachloride (6.37 mL, 58.1 mmol) was added, and the mixture was stirred for 10 min. Diisopropylethylamine (10.12 mL, 58.1 mmol) was added, and the mixture was stirred for 1 h at −78° C. A 1 M solution of hex-5-enal (58.1 mL, 58.1 mmol) in dichloromethane was added, and the mixture was stirred for 2 h at −78° C. The reaction was quenched by addition of half-saturated NH4Cl (30 mL) and warmed to room temperature. The mixture was extracted twice with dichloromethane, and the organic phase was dried and evaporated to provide a residue. Chromatography on silica gel afforded the title compound (12.92 g, 74%). This procedure has also been carried out using the (R)-1-(4-benzyl-2-thioxothiazolidin-3-yl)ethanone auxiliary, with a similar result.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07320974B2
出典データセットuspto-grants-2008_01
ORD IDord-538157f1bdb54ee8ada57adc71242da2
出典メモuspto-grants-2008_01