Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Diethyl Ether → 1-Naphthol
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Diethyl Ether | HCID 3283 | — |
| 반응물 | Duloxetine | HCID 60835 | — |
| 생성물 | 1-Naphthol | HCID 7005 | — |
| 생성물 | Thiophen-2-ol | HCID 10909502 | — |
반응 단계
Duloxetine is acid labile, and acid hydrolysis of its ether linkage results in a thienyl alcohol and 1-naphthol. 50% of a dosage is hydrolyzed to 1-naphthol within one hour at a pH of 1.0, which is achieved under fasting conditions. At a pH of 2.0, 10% of the dosage degrades to 1-Naphthol in one hour and at a pH of 4.0, 10% degradation would take up to 63 hours. The reaction scheme showing the conversion of duloxetine to 1-naphthol and its thienyl derivative is shown below.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08093408B2 |
| 출처 데이터셋 | uspto-grants-2012_01 |
| ORD ID | ord-de1aac75d8c34331899b85869fa93e77 |
| 출처 메모 | uspto-grants-2012_01 |