참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 1-(Chloromethoxy)-2-methoxyethane | HCID 77590 | — |
| 반응물 | Methyl 6-hydroxy-2-naphthoate | HCID 390995 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | Methyl 6-(2-methoxyethoxymethoxy)naphthalene-2-carboxylate | HCID 12085484 | 85% |
반응 단계
3.3 g (83 mmol) of 60% sodium hydride in oil are added portionwise to a solution of 14 g (69 mmol) of methyl 6-hydroxynaphthalene-2-carboxylate in 180 ml of an equivolume mixture of tetrahydrofuran and dimethylformamide. After the evolution of gas has ceased, 8.7 ml (76 mmol) of methoxyethoxymethyl chloride are added dropwise. The reaction medium is stirred at room temperature for 3 hours, immersed into ice-cold water and extracted with ethyl ether. The organic phase is dried over sodium sulfate, filtered and concentrated under vacuum. The residue obtained is purified by chromatography on a column of silica eluted with an 80/20 heptane/ethyl acetate mixture. 17 g of methyl 6-(2-methoxyethoxymethoxy)naphthalene-2-carboxylate are obtained in the form of a colorless oil, in a yield of 85%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07125869B2 |
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| 출처 데이터셋 | uspto-grants-2006_10 |
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| ORD ID | ord-561eae2879104e1584fc2cf404214913 |
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| 출처 메모 | uspto-grants-2006_10 |
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