참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Isobutylene | HCID 8255 | — |
| 반응물 | 3-Bromobenzaldehyde | HCID 76583 | — |
| 반응물 | Ytterbium triflate | HCID 2733225 | — |
| 반응물 | 4-Amino-3-methylbenzonitrile | HCID 7010316 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 2-(3-Bromophenyl)-4,4,8-trimethyl-1,2,3,4-tetrahydroquinoline-6-carbonitrile | HCID 67289987 | 26.2% |
반응 단계
To a stirred solution of 4-amino-3-methyl-benzonitrile (10.3 g, 78.4 mmol) and 3-bromobenzaldehyde (9.2 mL, 78.4 mmol) in acetonitrile (150 mL) were added isobutene (21.0 mL, 313.5 mmol) and ytterbium(III) trifluoromethanesulfonate (Yb(OTf)3) (5.8 g, 9.5 mmol). The resulting mixture was stirred at 85° C. for 18 h in sealed tube. The mixture was diluted with ethyl acetate (300 mL) and washed with water (100 mL×2) and brine (100 mL×2) and then dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the residue was purified by ISCO combi-flash chromatography (gradient elution, 10-30% ethyl acetate in petroleum ether) to afford 2-(3-bromo-phenyl)-4,4,8-trimethyl-1,2,3,4-tetrahydro-quinoline-6-carbonitrile (7.3 g, 26.1%) as a light yellow oil: LC/MS m/e obsd. (ESI+) [(M+H)+] 355.0 & 357.0.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08546427B2 |
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| 출처 데이터셋 | uspto-grants-2013_10 |
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| ORD ID | ord-1d2e55a5f4514e8b9eb0a1c1afb69f7f |
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| 출처 메모 | uspto-grants-2013_10 |
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