참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | P-Cresol | HCID 2879 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Thionyl Chloride | HCID 24386 | — |
| 반응물 | 2,4,5-Trifluorobenzoic acid | HCID 521170 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 4-Methylphenyl 2,4,5-trifluorobenzoate | HCID 58042408 | 66.4% |
반응 단계
Thionyl chloride (50 mL, 680 mmol) was added to 2,4,5-trifluorobenzoic acid (10 g, 57 mmol) and the mixture stirred at 55° C. for 18 hours. After cooling, the excess thionyl chloride was removed in vacuo. The resulting crude oil was azeotroped twice with DCM (30 mL) and toluene (20 mL) and the residue redissolved in DCM (50 mL), then cooled to 0° C. with an ice bath. A mixture of 4-methylphenol (6.4 g, 59 mmol) and triethylamine (10 mL, 71 mmol) in DCM (20 mL) was added over 30 minutes. The reaction was allowed to warm up to room temperature over 1 hour. The crude reaction mixture was partitioned between EtOAc (200 mL) and saturated sodium bicarbonate solution (70 mL). The aqueous layer was separated and extracted with EtOAc (100 mL). The combined organic extracts were combined, washed with saturated sodium bicarbonate solution (70 mL) and water (100 mL), dried over magnesium sulfate and concentrated in vacuo to provide a crude solid, which was purified by silica gel chromatography eluting with 5% EtOAc in heptane to provide the title compound (10.08 g, 66%) as a white solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US08685977B2 |
|---|
| 출처 데이터셋 | uspto-grants-2014_04 |
|---|
| ORD ID | ord-23bc6e40bbd346c4917fbb9d6c8a2ba8 |
|---|
| 출처 메모 | uspto-grants-2014_04 |
|---|