참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Propargyl bromide | HCID 7842 | — |
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | 1,4-Benzenedimethanol | HCID 11506 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 4-[(2-Propynyloxy)methyl]benzyl alcohol | HCID 54520131 | 58% |
반응 단계
To a mixture of sodium hydride (400 mg, 8.4 mmol, 50% in oil) and tetrahydrofuran (30 mL) was added 1,4-benzenedimethanol (2.3 g, 17 mmol) at 0° C., and then N,N-dimethylformamide (30 mL) was added. The reaction mixture was stirred at room temperature for 10 minutes, after which propargyl bromide (1.0 g, 8.4 mmol) was added dropwise to the reaction mixture at 0° C. The reaction mixture was stirred at room temperature for 1 hour, after which water was added to the reaction mixture, which was extracted with ethyl acetate. The organic layer was washed and saturated aqueous sodium chloride, and was concentrated under a reduced pressure. The residue thus obtained was purified by NH silica gel column chromatography (heptane:ethyl acetate=3:2) to obtain the title compound (860 mg, 58%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07691882B2 |
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| 출처 데이터셋 | uspto-grants-2010_04 |
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| ORD ID | ord-069a5b2d59254c22abe480ca278edf54 |
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| 출처 메모 | uspto-grants-2010_04 |
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