참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methanesulfonic Acid | HCID 6395 | — |
| 반응물 | Phthalaldehydic acid | HCID 8406 | — |
| 반응물 | Sodium Methoxide | HCID 10942334 | — |
| 반응물 | Dimethylphosphite | HCID 21884954 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | Dimethyl (3-oxo-1,3-dihydro-2-benzofuran-1-yl)phosphonate | HCID 11118213 | — |
반응 단계
Dimethyl phosphite (22.0 g, 0.2 mol) was added drop-wise to a solution of sodium methoxide (43.0 g) in methanol (100 ml) at 0° C. 2-Carboxybenzaldehyde (21.0 g, 0.1 mol) was then added portion-wise to the reaction mixture as a slurry in methanol (40 ml), with the temperature kept below 5° C. The resulting pale yellow solution was warmed to 20° C. over 1 hour. Methanesulphonic acid (21.2 g, 0.22 mol) was added to the reaction drop-wise and the resulting white suspension was evaporated in vacuo. The white residue was quenched with water and extracted into chloroform (3×100 ml). The combined organic extracts were washed with water (2×100 ml), dried over MgSO4, and evaporated in vacuo to yield (3-oxo-1,3-dihydro-isobenzofuran-1-yl)phosphonic acid dimethyl ester as a white solid (32.0 g, 95%, 95% purity). This was then used without further purification in the next stage.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07449464B2 |
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| 출처 데이터셋 | uspto-grants-2008_11 |
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| ORD ID | ord-6ff759119ac540f0b5fd1dceb834ca69 |
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| 출처 메모 | uspto-grants-2008_11 |
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