참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | 4-Bromo-6,7-dihydro-8(5H)-isoquinolinone | HCID 71743380 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 4-Bromo-5,6,7,8-tetrahydroisoquinolin-8-OL | HCID 71743891 | 92% |
반응 단계
4-Bromo-6,7-dihydroisoquinolin-8(5H)-one (2.135 g, 9.44 mmol) was suspended in MeOH (18.9 mL), cooled to 0° C. and treated with NaBH4 (357 mg, 9.44 mmol) in 5 portions over 30 min; then, the reaction was stirred for ¾ h at 0° C. (TLC after 30 min showed no more starting material). AcOH was then added dropwise until pH˜5-6 and the reaction mixture was evaporated. The residue was diluted with water and poured on aq. sat. NaHCO3-sol. followed by extraction with EtOAc (3×). The organic layers were washed once with aq. sat. NaHCO3-sol. and aq. 10% NaCl-sol., dried over Na2SO4 and concentrated in vacuo. The residue was re-dissolved in CH2Cl2, evaporated with n-pentane (3×) to around 20 ml each time, while the product precipitates; then, the solvent was decanted and the residue washed with n-pentane and dried in high vacuum to afford the title compound (1.98 g, 92%) as dark brown viscous oil. MS: 227 (M+, 1Br).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09133158B2 |
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| 출처 데이터셋 | uspto-grants-2015_09 |
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| ORD ID | ord-db24f0db5e9d4da5bd208f79b28e0016 |
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| 출처 메모 | uspto-grants-2015_09 |
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