Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Hydrochloric Acid → Methyl (3-butyl-1,2,4-oxadiazol-5-yl)benzoate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Cesium carbonate | HCID 10796 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 4-[5-[4-[(E)-N'-hydroxycarbamimidoyl]phenoxy]pentoxy]benzamidine | HCID 6505340 | — |
| 반응물 | Monomethyl terephthalate chloride | HCID 22493623 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Water methylene chloride | HCID 21908982 | — |
| 생성물 | Methyl (3-butyl-1,2,4-oxadiazol-5-yl)benzoate | HCID 54556725 | 93% |
반응 단계
Diisopropylethylamine (1.1 ml, 6.0 mmol) was added to a solution of terephthalic acid, monomethyl ester chloride (1.0 g, 5.0 mmol) and N-hydroxypentamidine (0.70 g, 6.0 mmol) in THF (8 mL). After stirring at ambient temperature for 1 hour, cesium carbonate (3.6 g, 11 mmol) was added and the reaction was stirred at 50° C. After stirring at 50° C. for 3.5 hours, the reaction was transferred to a separatory funnel with CH2Cl2/H2O. The aqueous layer was acidified with 1N HCl to pH 1 and extracted with CH2Cl2 (3×40 mL). The combined organic layers were dried (MgSO4) and concentrated in vacuo. Flash chromatography (silica, 50 mm dia, 10% EtOAc/hexane) afforded 1.2 g (93%) of methyl (3-butyl-1,2,4-oxadiazol-5-yl)benzoate.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06624309B1 |
| 출처 데이터셋 | uspto-grants-2003_09 |
| ORD ID | ord-9b1409d8ba994d1b8bd54e385b21a54a |
| 출처 메모 | uspto-grants-2003_09 |