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HRID 63985作成日:2026年10月25日

Acetic Acid → (3R,5R)-5-(3-fluorophenyl)pyrrolidin-3-ol

https://huagongshe.com/reaction/63985

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Sodium borohydrideHCID 4311764—
反応物(R)-3-(tert-butyldimethylsilyloxy)-5-(3-fluorophenyl)-3,4-dihydro-2H-pyrroleHCID 66847764—
溶媒MethanolHCID 887—
生成物(3R,5R)-5-(3-fluorophenyl)pyrrolidin-3-olHCID 6733007095%

反応手順

(R)-3-(tert-butyldimethylsilyloxy)-5-(3-fluorophenyl)-3,4-dihydro-2H-pyrrole (5.0 g, 17.0 mmol) was dissolved in 50 mL methanol and 10 mL AcOH and cooled to −40° C. NaBH4 (1.6 g, 43 mmol) was slowly added in small portions. The reaction was allowed to warm to ambient temperature. Most of the solvent was removed by rotary evaporation. The reaction was taken up in 200 mL of EtOAc, washed with 1 N NaOH, and filtered through Phase Separator filter paper, and concentrated. The crude product was taken up in 20 mL of 2 N HCl in dioxane. The reaction was concentrated, taken up in 200 mL of EtOAc, washed with 1 N NaOH, filtered, and concentrated, yielding the crude product, which was carried to the next step without further purification (2.93 g, 95% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09447104B2
出典データセットuspto-grants-2016_09
ORD IDord-be1c1ece2a1a45a8bf1cb39f4cf2d266
出典メモuspto-grants-2016_09