참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Iodoform | HCID 6374 | — |
| 반응물 | Butyl nitrite | HCID 10996 | — |
| 반응물 | 3-Amino-4-(trifluoromethyl)benzoic acid | HCID 642651 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 4-Carboxy-2-iodobenzotrifluoride, 3-Iodo-alpha,alpha,alpha-trifluoro-p-toluic acid | HCID 59318424 | — |
반응 단계
3-Amino-4-(trifluoromethyl)benzoic acid (commercially available) (6.5 g, 31.7 mmol) and triiodomethane (37.4 g, 95.1 mmol) were dissolved in THF (300 ml). The reaction mixture was heated to 80° C. and then butyl nitrite (5.56 ml, 47.6 mmol) was added slowly at this temperature. Heating was continued at this temperature for 4 hours and then the reaction was concentrated in vacuo to give the crude product. Purification by column chromatography (hexane to 30% EtOAc in hexane). This material was combined with another batch from a similar reaction performed on 2 g of 3-amino-4-(trifluoromethyl)benzoic acid. The combined material was purified by preparative HPLC to give the title compound (6.1 g). MS C8H4F3IO2 requires 316; found 315 (M−H+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US08101775B2 |
|---|
| 출처 데이터셋 | uspto-grants-2012_01 |
|---|
| ORD ID | ord-8c22aa50f5d6404d9219efda24c2f897 |
|---|
| 출처 메모 | uspto-grants-2012_01 |
|---|