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HRID 328895作成日:2026年10月25日

1-Naphthol → 1-(alpha-Naphthoxy)-2-benzyloxy-3-(iso-propylamino)-propane

https://huagongshe.com/reaction/328895

反応式

関与物質

役割名称HCID仕込み量
反応物1-NaphtholHCID 7005—
反応物Sodium HydroxideHCID 14798—
反応物1-(Iso-propyl)-3-benzyloxyazetidineHCID 20517324—
溶媒Diethyl EtherHCID 3283—
生成物1-(alpha-Naphthoxy)-2-benzyloxy-3-(iso-propylamino)-propaneHCID 1305570879%

反応条件

温度200 °C

反応手順

To a mixture of 6.2 parts of 1-(iso-propyl)-3-benzyloxyazetidine and 43 parts of α-naphthol 1.5 parts of sodium hydroxide was added, and the mixture was heated at 200° C. for 16 hours. The reaction mixture was cooled, and 100 parts of ether were added thereto. Excessive α-naphthol was removed by extraction with 2N-sodium hydroxide aqueous solution. The remaining ether layr was washed in water and dried over anhydrous sodium sulfate. After distillation of ether, the residue was subjected to distillation to yield 8.3 parts of 1-(α-naphthoxy)-2-benzyloxy-3-(iso-propylamino)-propane boiling at 192°-195° C. The yield was 79%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04018824
出典データセットuspto-grants-1977_04
ORD IDord-08d8eafb95d447d1a0a5fec4a5d9df11
出典メモuspto-grants-1977_04