참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 1-(Chloromethoxy)-2-methoxyethane | HCID 77590 | — |
| 반응물 | Methyl 6-hydroxy-2-naphthoate | HCID 390995 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Methyl 6-(2-methoxyethoxymethoxy)naphthalene-2-carboxylate | HCID 12085484 | — |
반응 단계
14 g (69 mmol) of methyl 6-hydroxynaph-thalene-2-carboxylate in 90 ml of dimethylformamide and 90 ml of tetrahydrofuran are introduced into a round-bottomed flask and under a nitrogen stream. 3.3 g (82 mmol) of sodium hydride at 60% are added in small portions. When the gas emission has ceased, 8.7 ml (76 mmol) of 2-methoxyethoxymethyl chloride are added and the reaction medium is stirred for 3 hours at room temperature. It is then poured into ice-cold water and extracted with ether. The organic phase is dried over magnesium sulphate, filtered and evaporated off. The residue obtained is purified by chromatography on a silica column eluted with a heptane and ethyl acetate (80/20) mixture and 17 g (85%) of the expected product are obtained in the form of a colorless oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06908939B2 |
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| 출처 데이터셋 | uspto-grants-2005_06 |
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| ORD ID | ord-eb23a3d8fea94d1780e4a9ebee2e96e5 |
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| 출처 메모 | uspto-grants-2005_06 |
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