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HRID 568983作成日:2026年10月25日

Hydrochloric Acid → 3-Amino-4,4-difluoro-7-methoxy-1-heptene

https://huagongshe.com/reaction/568983

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Sodium borohydrideHCID 4311764—
反応物2,2-Difluoro-5-methoxyvaleronitrileHCID 14097600—
反応物HCID 178418507HCID 178418507—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物3-Amino-4,4-difluoro-7-methoxy-1-hepteneHCID 20149450—

反応条件

温度-12 °C

反応手順

Under an atmosphere of nitrogen, 2,2-difluoro-5-methoxyvaleronitrile (4.85 mg, 3.25 mmoles), dissolved in tetrahydrofuran (5 ml), is slowly added to vinyl magnesium bromide (8 ml, 0.5M in tetrahydrofuran, 4 mmoles) previously cooled to -12° C. The reaction mixture is kept at -10° C. for 1/2 hour and then cooled to -40° C. A solution/suspension of sodium borohydride (133 mg, 3.5 mmoles) in methanol (14 ml) and water (0.5 ml), cooled to -40° C., is poured into the mixture, The temperature is allowed to rise to 0° C., and the mixture kept at this temperature for 10 min. The mixture is acidified with 6N HCl and concentrated under reduced pressure. The residue is dissolved in water, the aqueous solution is extracted twice to remove by-products, made alkaline with 4N NaOH, saturated with sodium chloride, and extracted again twice with ether. Usual work-up gives the title compound as a yellowish oil which is used for the next step without further purification: 420 mg (70)%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04730006
出典データセットuspto-grants-1988_03
ORD IDord-0888395cb0ee432e9f6aac7581d7f33f
出典メモuspto-grants-1988_03