참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dichloromethane | HCID 6344 | — |
| 반응물 | 1,2,3,4-Tetrahydroisoquinoline | HCID 7046 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Potassium Persulfate | HCID 24412 | — |
| 촉매 | Nickel sulfate hexahydrate | HCID 5284429 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 3,4-Dihydroisoquinoline | HCID 76705 | — |
반응 단계
Into a 5000 ml, 3-neck round-bottom flask equipped with a mechanical stirrer is placed 1,2,3,4-tetrahydroisoquinoline (1) (25.005 g) and methylene chloride (750 ml). A solution of potassium persulfate (71.376 g) and sodium hydroxide (18.0456 g) in deionized water (1650 ml) is added. While vigorously stirring the biphasic mixture, a solution of nickel sulfate hexahydrate (0.6499 g) in deionized water (75 ml) is added dropwise to the mixture. The reaction is allowed to stir overnight at room temperature. The biphasic mixture is vacuum filtered through Celite, the phases separated and the water layer extracted (3×300 ml) with methylene chloride. The organics are combined, dried with MgSO4 and reduced by rotary evaporation to a thick, dark brown oil. The desired product is isolated from the oil by Kugelrohr distillation (0.1 mm Hg, 75° C.). The preparation is represented by the following reaction: ##STR26##
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05710116 |
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| 출처 데이터셋 | uspto-grants-1998_01 |
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| ORD ID | ord-866a01512fa14a7a81855cbc5990170c |
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| 출처 메모 | uspto-grants-1998_01 |
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