戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1414作成日:2026年10月26日

Hydrochloric Acid → 6-Benzyloxy-1,2,3,4-tetrahydro-naphthalene-2-carboxylic Acid

https://huagongshe.com/reaction/1414

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Benzyl BromideHCID 7498—
反応物Potassium HydroxideHCID 14797—
反応物6-Hydroxy-1,2,3,4-tetrahydronaphthalene-2-carboxylic acidHCID 19070001—
触媒Sodium IodideHCID 5238—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物6-Benzyloxy-1,2,3,4-tetrahydro-naphthalene-2-carboxylic AcidHCID 1906997392.8%

反応条件

温度100 °C

反応手順

A mixture of 10.60 g (50 mmol) of 1,2,3,4-tetrahydro-6-hydroxynaphthalene-2-carboxylic acid, 12.85 g (75 mmol) of benzyl bromide, 6.6 g (100 mmol) of 85% potassium hydroxide, 0.525 g (3.5 mmol) of sodium iodide, 200 ml of ethanol and 25 ml of distilled water was heated under reflux at 100° C. for 12 hours. To this reaction mixture was added 50 ml of 10% potassium hydroxide, followed by heating under reflux at that temperature for 2 hours. After allowing the reaction system to cool up to room temperature, the reaction mixture in cold water was acidified with 36% hydrochloric acid. The resulting deposited product was filtered, and recrystallized from toluene to obtain 13.08 g (46.4 mmol) of 1,2,3,4-tetrahydro-6-benzyloxynaphthalene-2-carboxylic acid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05725798
出典データセットuspto-grants-1998_03
ORD IDord-7d2c74c555f047899e0fbc54d1163d31
出典メモuspto-grants-1998_03