Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Lithium Chloride → 4-Cyano-2-(2-phenylethynyl)benzaldehyde
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Lithium Chloride | HCID 433294 | — |
| 반응물 | Tris(furan-2-yl)phosphane | HCID 521585 | — |
| 반응물 | Tributyl(2-phenylethynyl)stannane | HCID 630640 | — |
| 반응물 | 4-Cyano-2-trifluoromethylsulphonylbenzaldehyde | HCID 54002071 | — |
| 용매 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 생성물 | 4-Cyano-2-(2-phenylethynyl)benzaldehyde | HCID 54356802 | — |
반응 단계
A mixture of 4-cyano-2-trifluoromethylsulphonyl-benzaldehyde (1.75 g, 6.3 mmol), tris(dibenzylidenacetone)dipalladium(o) (116 mg, 0.13 mmol), tris(2-furyl)phosphine (234 mg, 1.0 mmol) and anhydrous lithium chloride (0.8 g, 18.9 mmol) in dry N-methyl pyrrolidinone (18 ml) were reacted with (phenylethynyl)tri-n-butyltin (2.91 g, 7.4 mmol) for 3 hours at 50° C. and worked up following the procedure described in Example 15 (i). The crude oil was chromatographed on flash silica eluting with hexane-diethyl ether (4:1) to give 4-cyano-2-(2-phenylethynyl)benzaldehyde as a yellow solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05863947 |
| 출처 데이터셋 | uspto-grants-1999_01 |
| ORD ID | ord-2fe22a9cfc544a6bbcdf55fe959a3660 |
| 출처 메모 | uspto-grants-1999_01 |