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HRID 2350作成日:2026年10月23日

Hexamethyldisilazane → 1-(3-Indanyloxy-4-methoxyphenyl)propylamine

https://huagongshe.com/ja/reaction/2350

反応式

関与物質

役割名称HCID仕込み量
反応物HexamethyldisilazaneHCID 13838—
反応物Ammonium ChlorideHCID 25517—
反応物3-Indanyloxy-4-methoxybenzaldehydeHCID 57257970—
反応物ButyllithiumHCID 178418339—
反応物HCID 178418443HCID 178418443—
溶媒AcetonitrileHCID 6342—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物1-(3-Indanyloxy-4-methoxyphenyl)propylamineHCID 570150489%

反応手順

To an ice bath cooled stirred solution of 1,1,1,3,3,3-hexamethyldisilazane (2.7 mL, 13 mmol) in tetrahydrofuran (5 mL) under nitrogen, was added a hexane solution of butyl lithium (2.5M, 4.8 mL, 12 mmol) via syringe. The ice bath was removed and the solution was stirred for 25 minutes at room temperature. This solution then was added dropwise to an ice bath cooled solution of 3-indanyloxy-4-methoxybenzaldehyde (2.68 g, 10.0 mmol) in tetrahydrofuran (4 mL) and the mixture was stirred for one hour. An ethereal solution of ethylmagnesium bromide (3M, 6.7 mL, 20 mmol) then was added dropwise via syringe. The reaction mixture was heated at reflux and was monitored by HPLC (Waters Nova-Pak/EC 18 column, 3.9×150 mm, 4 micron, 1 mL/min, 240 nm, 40/60, CH3CN/0.1% H3PO4 (aq)). After 48 hours the reaction had reached completion and was allowed to cool to room temperature. The reaction mixture then was slowly poured into a saturated solution of ammonium chloride (80 mL). The resulting mixture was extracted with methylene chloride (3×15 mL) and the combined extracts were dried over magnesium sulfate and concentrated to afford the product which was further purified by flash column chromatography (silica gel, 250/10/1, methylene chloride/methanol/ammonium hydroxide) to afford 0.27 g (9%) of product as an orange solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05728844
出典データセットuspto-grants-1998_03
ORD IDord-a172f4e4b1614e5bac954c6d01d97ff6
出典メモuspto-grants-1998_03