Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2-Mercaptoethanol → 3'-(2-Hydroxy-ethylsulfanylmethyl)-biphenyl-4-carboxylic acid ethyl ester
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2-Mercaptoethanol | HCID 1567 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 4'-(2-Hydroxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid ethyl ester | HCID 58610579 | — |
| 반응물 | 3'-Bromomethyl-biphenyl-4-carboxylic acid ethyl ester | HCID 58610587 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 3'-(2-Hydroxy-ethylsulfanylmethyl)-biphenyl-4-carboxylic acid ethyl ester | HCID 58610598 | — |
반응 단계
3′-(2-Hydroxy-ethylsulfanylmethyl)-biphenyl-4-carboxylic acid ethyl ester was synthesized as described for 4′-(2-hydroxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid ethyl ester. 3′-Bromomethyl-biphenyl-4-carboxylic acid ethyl ester (4.98 g, 15.6 mmol, 1 eq) in anhydrous DMF was treated with 2-mercaptoethanol (2.44 g, 31.20 mmol, 2 eq.) and potassium carbonate (6.47 g, 46.80 mmol, 3 eq.). When complete, the reaction was worked up as described leaving a yellow oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07132456B2 |
| 출처 데이터셋 | uspto-grants-2006_11 |
| ORD ID | ord-f3ea096d400641448c348262cbcd3c2a |
| 출처 메모 | uspto-grants-2006_11 |