関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triethyl Phosphate | HCID 6535 | — |
| 反応物 | 4-(Bromomethyl)indan-1-one | HCID 18694050 | — |
| 反応物 | Diethyl 1-oxoindan-4-ylmethylphosphonate | HCID 18694052 | — |
| 溶媒 | O-Xylene | HCID 7237 | — |
| 生成物 | Diethyl (2-bromo-1-oxoindan-4-yl)methylphosphonate | HCID 18694081 | — |
反応手順
The diethyl 1-oxoindan-4-ylmethylphosphonate can be prepared in the following manner: a mixture of 0.5 g of 4-(bromomethyl)indan-1-one, 0.9 g of triethyl phosphate and 5 ml of xylene is heated at reflux for 5 hours. The reaction medium is concentrated in a rotary evaporator and then the residue is purified by chromatography on silica, eluting with an ethyl acetate-petroleum ether (85-15 by volume) mixture. 0.4 g of diethyl (2-bromo-1-oxoindan-4-yl)methylphosphonate is obtained in the form of a colourless oil [1H NMR spectrum in DMSO-d6, T=300K, δ in ppm (250 MHz): 1.20 (6H, t, J=6 Hz, 2 CH3), 2.70 (2H, m, CH2CO), 3.20 (2H, m, CH2), 3.38 (2H, d, J=22 Hz, PCH2), 4.00 (2H, q, J=6 Hz, OCH2), 7.45 (1H, t, J=7 Hz, arom. CH), 7.60 (2H, m, 2 arom. CH)].
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05990108 |
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| 出典データセット | uspto-grants-1999_11 |
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| ORD ID | ord-b7df19c71dfd4ac08ec2c1bc2afb2632 |
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| 出典メモ | uspto-grants-1999_11 |
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