참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3-Bromophenol | HCID 11563 | — |
| 반응물 | Pentyl ether | HCID 12743 | — |
| 반응물 | Benzyl 5-Bromoamyl Ether | HCID 14221121 | — |
| 반응물 | 3-(Benzyloxypentyl)-phenol | HCID 53906938 | — |
| 반응물 | HCID 178418306 | HCID 178418306 | — |
| 촉매 | Palladium | HCID 23938 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Pentyl ether | HCID 12743 | — |
| 생성물 | 3-(5-Hydroxypentyl)-phenol | HCID 22407972 | — |
반응 단계
At a temperature of -78° C., 19.4 ml of t-butyl lithium (1.7M) is added to 4.0 gm of the above 3-bromo-phenol, n-pentyl ether in 50 mls tetrahydrofuran; and to this is added 3.3 ml of a freshly prepared solution of Li2CuCl3 (0.10M/THF). The mixture is stirred for 10 minutes, and then 4.35 grams of the 1-bromo-5-benzyloxy pentane are added. The reaction is allowed to warm slowly to ambient temperature over 12 hours and is then stirred an additional 24 hours before being quenched with silica gel. After removing the solvent, the mixture is chromatographed over silica gel (1:1 hexane:ether) to yield a crude mixture containing 3-(benzyloxypentyl)-phenol, n-pentyl ether. A solution of 6.0 gm of this crude mixture in ethanol is hydrogenated over 5% Pd on carbon for 5 hours. After filtering through celite and concentrating, pure 3-(5-hydroxypentyl)-phenol, n-pentyl ether is obtained as a clear oil by HPLC chromatography.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05412137 |
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| 출처 데이터셋 | uspto-grants-1995_05 |
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| ORD ID | ord-a33eb14b5e2546bc96b1dbc59ac08fd1 |
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| 출처 메모 | uspto-grants-1995_05 |
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