참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Diethyl Oxalate | HCID 7268 | — |
| 반응물 | Ethyl 4-(2-bromo-5-methoxy phenyl)butyrate | HCID 15662398 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | 2-Oxo-3-carboethoxy-5-(2-bromo-5-methoxyphenyl)pentanoic acid ethyl ester | HCID 15662399 | 89% |
반응 단계
Potassium t-butoxide (26.94 g) was suspended in 130 ml of anhydrous ether and cooled to 0° C. A solution of 60.24 g ethyl -4-(2-bromo-5-methoxy phenyl)butyrate and 43.84 g diethyl oxalate in 60 ml ether was added dropwise over 20 min. After 2 h at 25° C., the reaction was poured into 400 ml H2O and the aqueous layer was separated, acidified to pH 1 and extracted with ether. The ether layer was dried (MgSO4) and the solvent was evaporated to yield 71.26 g of the desired product as a colorless oil (89%). NMR (CDCl3) δ 1.25 (t, 3H), 1.4 (t, 3H), 2.25 (m, 2H), 2.75 (m, 2H), 3.78 (s, 3H), 4.0-4.5 (m, 5H), 6.64 (dd, 1H), 6.79 (d, 1H), 7.40 (d, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US05244888 |
|---|
| 출처 데이터셋 | uspto-grants-1993_09 |
|---|
| ORD ID | ord-623055db120040d483ebba9a6496e49a |
|---|
| 출처 메모 | uspto-grants-1993_09 |
|---|