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HRID 855177作成日:2026年10月24日

4-tert-Butylbenzylamine → (4-Tert-butyl-benzyl)-[2-(tetrahydro-thiopyran-4-yl)-ethyl]-amine

https://huagongshe.com/ja/reaction/855177

反応式

関与物質

役割名称HCID仕込み量
反応物4-tert-ButylbenzylamineHCID 2735655—
反応物Sodium borohydrideHCID 4311764—
反応物(Tetrahydro-thiopyran-4-YL)-acetaldehydeHCID 23532962—
触媒Hydrochloric AcidHCID 313—
溶媒MethanolHCID 887—
生成物(4-Tert-butyl-benzyl)-[2-(tetrahydro-thiopyran-4-yl)-ethyl]-amineHCID 6934200587%

反応手順

0.44 ml of 4-tert-butylbenzylamine (2.5 mmol) and 541 mg (tetrahydro-thiopyran-4-yl)-acetaldehyde (3.75 mmol) were dissolved in 7.5 ml methanol and stirred for 30 min at rt and then refluxed for 2.5 h. After cooling down to rt, 114 mg (3 mmol) of sodium borohydride were added and after stirring for 15 min at rt, the reaction mixture was refluxed for 2¾ h. After cooling down to rt, the reaction mixture was treated with 5 drops 1 N HCl and concentrated in vacuo. The residue was diluted with water/EtOAc. After separation of the organic phase, the aqueous phase was extracted with EtOAc and the combined organic phases were washed with brine, dried with magnesium sulfate, filtered off and concentrated in vacuo. The residue was purified by column chromatography (90 g silica gel; EtOAc/heptane 1:2 then EtOAc) to give 632 mg light yellow viscous oil (87%). MS (ISP) 292.3 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07259183B2
出典データセットuspto-grants-2007_08
ORD IDord-d72b0d96ae2c430e9a02ed5ef497f832
出典メモuspto-grants-2007_08