참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methane, dichloromethoxy- | HCID 21004 | — |
| 반응물 | 2,7-Dimethoxynaphthalene | HCID 77021 | — |
| 촉매 | Titanium Tetrachloride | HCID 24193 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 2,7-Dimethoxy-1-naphthaldehyde | HCID 293215 | — |
반응 단계
The 2,7-dimethoxynaphthalene 2 (65 mmol; 12.26 g) is dissolved in 150 cm3 of anhydrous dichloromethane under an inert atmosphere. TiCl4 (91 mmol; 10cm3) is added by syringe, at 0° C., followed by dropwise addition, by means of a dropping funnel, of α,α-dichloromethyl methyl ether (99 mmol; 9 cm3) in solution in 40 cm3 of the same solvent. Stirring is continued at 0° C. for 1 h and then at room temperature for 4 h 30. The reaction medium is poured onto an ice/3N HCl mixture (250 cm3), stirred vigorously and then extracted with CH2Cl2. The organic phase is washed with water and then with saturated NaHCO3 solution. The organic phase is dried over MgSO4 and evaporated. The residue is taken up in ether, the solution is filtered and the filtrate is evaporated to dryness. 2,7-Dimethoxynaphthaldehyde 3 is isolated pure in the form of a beige-colored powder.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05712312 |
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| 출처 데이터셋 | uspto-grants-1998_01 |
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| ORD ID | ord-d11bd4061662452d84eeab80fa1de7f5 |
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| 출처 메모 | uspto-grants-1998_01 |
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