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HRID 542344作成日:2026年10月26日

Pyridine → 9-(4-Methoxy-2,3,6-trimethyl-phenyl)-3,7-dimethyl-nona-2,4,6,8-tetraen-1-oic acid propargyl ester

https://huagongshe.com/reaction/542344

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Propargyl alcoholHCID 7859—
反応物Phosphorus trichlorideHCID 24387—
反応物9-(4-Methoxy-2,3,6-trimethylphenyl)-3,7-dimethyl-2,4,6,8-nonatetraenoic acidHCID 41317—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物9-(4-Methoxy-2,3,6-trimethyl-phenyl)-3,7-dimethyl-nona-2,4,6,8-tetraen-1-oic acid propargyl esterHCID 54137305—

反応手順

20 g of 9-(4-methoxy-2,3,6-trimethyl-phenyl)-3,7-dimethyl-nona-2,4,6,8-tetraen-1-oic acid are dissolved in 200 ml of tetrahydrofuran. After the addition of 5.5 ml of phosphorus trichloride, the solution is stirred for 2 hours at room temperature, cooled to 0° C. and treated firstly with 50 ml of pyridine and then dropwise at 0°-5° C. with 50 ml of propargyl alcohol. The mixture is stirred for 2 hours at room temperature and then diluted with water. The organic phase is washed successively with water, dilute hydrochloric acid and a 2% aqueous sodium bicarbonate solution, dried over sodium sulphate and evaporated. There is obtained 9-(4-methoxy-2,3,6-trimethyl-phenyl)-3,7-dimethyl-nona-2,4,6,8-tetraen-1-oic acid propargyl ester which melts at 94°-95° C. after absorption on aluminum oxide using benzene as the eluent.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04656310
出典データセットuspto-grants-1987_04
ORD IDord-302a803b462c47369ed747e5d63b1876
出典メモuspto-grants-1987_04