참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 1,3-Benzenedicarboxylic acid, 5-hydroxy-, 1,3-dimethyl ester | HCID 83065 | — |
| 반응물 | 4-Fluorophenylboronic acid | HCID 285645 | — |
| 반응물 | HCID 66616553 | HCID 66616553 | — |
| 촉매 | Cupric acetate | HCID 8895 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | Dimethyl 5-(4-fluorophenoxy)isophthalate | HCID 66616627 | 85% |
반응 단계
A mixture of dimethyl 5-hydroxyisophthalate (3.1 g, 14.75 mmol), 4-fluorophenylboronic acid (4.13 g, 29.5 mmol), copper(II) acetate (2.68 g, 14.75 mmol) and triethylamine (4.48 g, 44.2 mmol) in CH2Cl2 (65 mL) was stirred at rt in the open air for 38 h. An additional 1 g of fluorophenylboronic acid was added and the reaction mixture was continued to stir at rt in the open air. After 24 h, an additional 1 g of fluorophenylboronic acid and 300 mg of copper acetate were added to the reaction mixture and it was continued to stir for 6 h in the open air. The mixture was mixed with CHCl3 and aq HCl, the organic layer was separated, washed with aq HCl, aq NaHCO3, dried over MgSO4, concentrated, and the residue was purified by flash column chromatography on SiO2 eluting with Hexane:EtOAc:MeOH/800:200:40 to obtain the desired product (3.8 g, 12.49 mmol, 85% yield) as a white solid. 1H NMR (CDCl3): δ 8.36 (s, 1H), 7.75 (s, 2H), 7.06˜6.96 (m, 4H), 3.89 (s, 6H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US08501992B2 |
|---|
| 출처 데이터셋 | uspto-grants-2013_08 |
|---|
| ORD ID | ord-245c996330624509804f3899d4307b31 |
|---|
| 출처 메모 | uspto-grants-2013_08 |
|---|