참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Formaldehyde | HCID 712 | — |
| 반응물 | Phosphoric Acid | HCID 1004 | — |
| 반응물 | 1-Benzylnaphthalene | HCID 38074 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 1-Benzyl-2-chloromethylnaphthalene | HCID 22119573 | 32% |
반응 단계
1-Benzylnaphthalene (3.0 g; 13.7 mMol), as prepared above, formaldehyde (1.0 g; 35.7 mMol), glacial acetic acid (4.3 g; 71.7 mMol), concentrated hydrochloric acid (6.5 mL) and 85% phosphoric acid (4.3 mL) were combined and heated in an oil bath maintained at 90° C. for 4.5 hr. The reaction mixture was cooled, a small amount of water was added, and extraction was carried out with diethyl ether. The combined organic extractions were washed with sodium carbonate (10% aqueous), and brine; then dried over magnesium sulfate. The solvent was removed under reduced pressure, and the residue subjected to medium pressure chromatography on silica gel eluting with hexane. The product (1.18 g; 32% yield) was isolated as a colorless oil which subsequently crystallized.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US06160175 |
|---|
| 출처 데이터셋 | uspto-grants-2000_12 |
|---|
| ORD ID | ord-703b44c124f74a87a1d4ca06178ead62 |
|---|
| 출처 메모 | uspto-grants-2000_12 |
|---|