참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Glycerol | HCID 753 | — |
| 반응물 | 4-Acetylbiphenyl | HCID 7113 | — |
| 반응물 | Ethyl bromoacetate | HCID 7748 | — |
| 반응물 | Ammonium Hydroxide | HCID 14923 | — |
| 촉매 | Zinc | HCID 23994 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Trimethyl borate | HCID 8470 | — |
| 생성물 | 3-(4-Biphenylyl)-2-butenoic acid ethyl ester | HCID 54501672 | — |
반응 단계
6.45 g (0.1 mole) of activated zinc metal (20 mesh) is placed in a flask fitted with a septum inlet and a magnetic stirrer. The system is maintained under a nitrogen atmosphere and kept at a temperature of 25° C. on a water bath. A solution of 19.6 g (0.1 mole) of 4-acetylbiphenyl in 75 ml of dry tetrahydrofuran and 75 ml of trimethyl borate (distilled from calcium hydride) is injected and the mixture stirred. 11.1 ml (0.1 mole) of freshly distilled ethyl bromoacetate is injected in one shot and the mixture stirred at 25° C. for 12 hours. A mixture of 25 ml of concentrated ammonium hydroxide and 75 ml of glycerine is added, and the aqueous phase is separated and extracted thrice with 25 ml portions of diethyl ether. The combined organic extracts are dried over anhydrous magnesium sulphate and the diethylether removed on a rotary evaporator, the residue is vacuum distilled and the fraction distilling at 0.125 mn at 171°-172° C. is collected. Recrystallisation from petroleum ether yields the heading compound, substantially in trans form.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US04344966 |
|---|
| 출처 데이터셋 | uspto-grants-1982_08 |
|---|
| ORD ID | ord-22a95e6c2cb74ed18706d6a6ec9e84cd |
|---|
| 출처 메모 | uspto-grants-1982_08 |
|---|