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HRID 633918作成日:2026年10月26日

Water → 1-(Diphenylmethyl)-3-(pentylsulfonyl)azetidine

https://huagongshe.com/reaction/633918

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sulfuric AcidHCID 1118—
反応物Sodium BicarbonateHCID 516892—
反応物Potassium hydroxy sulfiteHCID 23707502—
反応物1-(Diphenylmethyl)-3-(pentylthio)azetidineHCID 67154644—
溶媒MethanolHCID 887—
生成物1-(Diphenylmethyl)-3-(pentylsulfonyl)azetidineHCID 6715459430%

反応手順

To a solution of 1-(diphenylmethyl)-3-(pentylthio)azetidine (228 mg, 0.70 mmol; which may be prepared as described in Step 2) in methanol (6.3 mL) and water (6.3 mL) was added H2SO4 1N (0.7 mL). The reaction mixture was stirred for 10 minutes, then oxone (1.08 g, 1.75 mmol) was added and the mixture stirred at room temperature for 12 h. A solution of saturated NaHCO3 (5 mL) was added and the mixture extracted with ethyl acetate. The two layers were separated and the organic washed with brine, dried over Na2SO4, filtered and concentrated. The crude was then purified on column chromatography (pentane/EtOAc, 100/0 then 90/10) to give the title product (75 mg, 30%) as a pale yellow oil. The less pure fraction (N-oxide) can be recycled in hydrogenolysis conditions.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09321769B2
出典データセットuspto-grants-2016_04
ORD IDord-d99fc2ffbd124c6c811b142a409c11c5
出典メモuspto-grants-2016_04