Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2-Acetylnaphthalene → 2-Naphthoic acid
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2-Acetylnaphthalene | HCID 7122 | — |
| 반응물 | 2-Naphthoic acid | HCID 7123 | — |
| 반응물 | Diboron | HCID 6328200 | — |
| 반응물 | Sodium Hypochlorite | HCID 23665760 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Diglyme | HCID 8150 | — |
| 생성물 | 2-Naphthoic acid | HCID 7123 | — |
| 생성물 | 2-Naphthalenemethanol | HCID 74128 | — |
반응 단계
2-Acetylnaphthalene is prepared by treating 2-(1-bromoethyl)naphthalene, prepared as described above, with sodium acetate in acetic acid to afford 2-(1-acetoxyethyl)naphthalene which upon base hydrolysis furnishes the 2-(1-hydroxyethyl)naphthalene. The latter is oxidized with an equivalent of chromium trioxide in glacial acetic acid, or 8N sulfuric acid and acetone to furnish 2-acetylnaphthalene. 2-Carboxynaphthalene is prepared from 2-acetylnaphthalene by treating the latter with aqueous sodium hypochlorite. The 2-carboxynaphthalene is treated with diborane in an ether, such as diglyme (diethyleneglycol dimethyl ether), to yield 2-hydroxymethylnaphthalene.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04009197 |
| 출처 데이터셋 | uspto-grants-1977_02 |
| ORD ID | ord-fee330c163c5406791381ec023d45b83 |
| 출처 메모 | uspto-grants-1977_02 |