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HRID 25119作成日:2026年10月26日

tert-Butanol → N-Cbz-4-[(2,3-Dihydroxypropyloxy)phenyl]butylamine

https://huagongshe.com/reaction/25119

反応式

関与物質

役割名称HCID仕込み量
反応物tert-ButanolHCID 6386—
反応物N-Methylmorpholine N-oxide monohydrateHCID 2724197—
反応物[4-(4-Allyloxyphenyl)butyl]carbamic acid benzyl esterHCID 11551825—
反応物Sodium BisulfiteHCID 23665763—
触媒Osmium TetroxideHCID 30318—
溶媒Propan-2-one--water (1/1)HCID 18366337—
生成物N-Cbz-4-[(2,3-Dihydroxypropyloxy)phenyl]butylamineHCID 1155979462%

反応手順

A solution of osmium tetroxide (50 mg, 0.2 mmol) in tert-butanol (8 mL) was added to a solution of 4-methylmorpholine N-oxide monohydrate (1.2 g, 9.1 mmol) in 100 mL (1:1) acetone/water solution and the mixture was stirred for 10 min at room temperature. After this time, 30 (3.1 g, 9.0 mmol) was added in 50 mL (1:1) acetone/water solution. The reaction mixture was stirred at room temperature overnight, then NaHSO3 (0.5 g) was added and the stirring was continued for 15 min. The acetone was evaporated and the pH was adjusted to 5.5 by the addition of 2N HCl then the mixture was extracted with ethyl acetate. The organic fraction was isolated, dried with sodium sulfate, and filtered through silica gel. Compound 31 (2.1 g, 62%) was isolated as a white solid after removing the solvent and drying under vacuum. 1H NMR (300 MHz, DMSO-d6) δ 1.48 (m, 2H), 1.50 (m, 2H), 2.46 (m, 2H), 3.00 (m, 2H), 3.43 (m, 2H), 3.80 (m, 2H), 3.93 (t, 1H), 4.66 (d, 1H), 4.99 (s, 2H), 6.82 (d, 2H), 7.07 (d, 2H), 7.26 (s, 1H), 7.33 (s, 5H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06858615B2
出典データセットuspto-grants-2005_02
ORD IDord-7aa58a624b334f989ea7484e39e0bc73
出典メモuspto-grants-2005_02