참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Bromotoluene | HCID 7805 | — |
| 반응물 | 1,1-Dibromoethane | HCID 11201 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | 4,4-Dimethyl-2-(2-methoxyphenyl)oxazoline | HCID 333189 | — |
| 반응물 | Magnesium | HCID 5462224 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 4,4-Dimethyl-2-(4'-methyl-2-biphenylyl)-2-oxazoline | HCID 688301 | 85.1% |
반응 단계
Tetrahydrofuran (200 ml) was added to 2.5 g (103 mmol) of flaky magnesium, followed by the addition of a small amount of dibromoethane under stirring. After the confirmation of bubbling, 13 ml (106 mmol) of 4-bromotoluene was dropwise added thereto. After the confirmation of the dissolution of the magnesium, the mixture was further stirred at room temperature for one hour. This reaction liquid was dropwise added to a solution of 10.0 g (48.7 mmol) of 4,4-dimethyl-2-(2'-methoxyphenyl)oxazoline in tetrahydrofuran (100 ml), followed by stirring for 12 hours. The reaction liquid was poured into a saturated aqueous solution of ammonium chloride, followed by the extraction with chloroform. After washing with water and drying, vacuum concentration was conducted. The residue was purified by silica gel column chromatography (a n-hexane/ethyl acetate system) to give 11.0 g of the title compound as a crystal (yield 85%). m.p.; 56°-59° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05618969 |
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| 출처 데이터셋 | uspto-grants-1997_04 |
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| ORD ID | ord-c2dbefa41b844817bc4dce80250238a3 |
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| 출처 메모 | uspto-grants-1997_04 |
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