돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1414생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/1414

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Benzyl BromideHCID 7498—
반응물Potassium HydroxideHCID 14797—
반응물6-Hydroxy-1,2,3,4-tetrahydronaphthalene-2-carboxylic acidHCID 19070001—
촉매Sodium IodideHCID 5238—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물6-Benzyloxy-1,2,3,4-tetrahydro-naphthalene-2-carboxylic AcidHCID 1906997392.8%

반응 조건

온도100 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05725798
출처 데이터셋uspto-grants-1998_03
ORD IDord-7d2c74c555f047899e0fbc54d1163d31
출처 메모uspto-grants-1998_03