참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Bromoanisole | HCID 11358 | — |
| 반응물 | Magnesium | HCID 5462224 | — |
| 반응물 | Ethyl 3-(3,4-methylenedioxyphenyl)1-oxoindene-2-carboxylate | HCID 18427631 | — |
| 반응물 | Ethyl (1RS) 1-Hydroxy-1-(methoxyphenyl)-3-(3,4-methylenedioxyphenyl)indene-2-carboxylate | HCID 18969641 | — |
| 반응물 | HCID 178489560 | HCID 178489560 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Ether tetrahydrofuran | HCID 21868444 | — |
| 생성물 | 1-(2-Methoxyphenyl)-3-(3,4-methylenedioxyphenyl)indane-2-carboxylic acid | HCID 18703900 | — |
반응 단계
Ethyl (1RS)-1-Hydroxy-1-(2-methoxyphenyl)-3-(3,4-methylenedioxyphenyl)indene-2-carboxylate. To dry magnesium turnings (81 mg, 3,4 mmol) under an argon atmosphere was added a solution of 2-bromoanisole (0.64 g, 3.4 mmol) in 5:1 THF/Et2O (3 ml). A portion of the resulting 2-methoxyphenyl magnesium bromide solution (0.45 ml, 0.51 mmol) was added dropwise to a solution of ethyl 3-(3,4-methylenedioxyphenyl)-1-oxoindene-2-carboxylate (100 mg, 0.34 mmol) in THF (6 ml) under an argon atmosphere at 0° C. After stirring for 15 min, the mixture was partitioned between 3M HCl and EtOAc. The organic extract was washed successively with H2O, 5% aqueous NaHCO3, H2O and saturated aqueous NaCl. The solvent was removed in vacuo, and the residue was purified by flash chromatography, eluting with 15% EtOAc/hexanes to afford the title compound. (100 mg, 68%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06271399B1 |
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| 출처 데이터셋 | uspto-grants-2001_08 |
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| ORD ID | ord-3c72d7f638d84ce8a77650922b6c27de |
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| 출처 메모 | uspto-grants-2001_08 |
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