Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Potassium Carbonate → 2-(4-Methoxy-benzenesulfonyl)-5-methyl-hex-4-enoic acid ethyl ester
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 18-Crown-6 | HCID 28557 | — |
| 반응물 | 2-[(4-Methoxyphenyl)sulfonyl]acetic acid ethyl ester | HCID 1482372 | — |
| 반응물 | Bromoisoprene | HCID 53976308 | — |
| 용매 | Acetone | HCID 180 | — |
| 생성물 | 2-(4-Methoxy-benzenesulfonyl)-5-methyl-hex-4-enoic acid ethyl ester | HCID 11759197 | — |
반응 단계
To a stirred solution of (4-methoxy-benzenesulfonyl)-acetic acid ethyl ester (5.16 g, 20 mmol), isoprenyl bromide (3.0 g, 20 mmol) and 18-Crown-6 (500 mg) in acetone (250 ml) was added K2CO3 (10 gms, excess) and the mixture refluxed foe 24 hours. At the end, the reaction mixture was filtered and the acetone layer was concentrated. The residue obtained was extracted with chloroform, washed well with water, dried over anhydrous MgSO4, filtered and concentrated. The product obtained was purified by silica-gel column chromatography, eluting with 30% ethy acetate: hexane. The product 2-(4-methoxy-benzenesulfonyl)-5-methyl-hex-4-enoic acid ethyl ester was isolated as a colourless oil. Yield: 3.0 g, 93%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06172057B2 |
| 출처 데이터셋 | uspto-grants-2001_01 |
| ORD ID | ord-38c567a749204ef4915213ea3d8356c1 |
| 출처 메모 | uspto-grants-2001_01 |