関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4,5-Dibromothiophene-2-carbaldehyde | HCID 813164 | — |
| 反応物 | Tert-butyl (diphenoxyphosphoryl)acetate | HCID 10689048 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | cis-3-(4,5-Dibromo-thiophen-2-yl)-acrylic acid tert-butyl ester | HCID 67205492 | — |
反応手順
(Diphenoxy-phosphoryl)-acetic acid tert-butyl ester (8.49 g, 24.4 mmol) was dissolved in THF (519 ml) and cooled to −78° C. followed by the addition of triton B (13.3 ml, 40% by wt. in MeOH). After 15 minutes a solution of 4,5-Dibromo-thiophene-2-carbaldehyde (7.0 g, 25.9 mmol) in THF (20 ml) was added and the reaction was stirred for 1 hour. Next, the reaction mixture was quenched with sat. NH4Cl (250 ml), diluted with H2O (500 ml), and extracted with EtOAc (2×300 ml). The organic layers were washed with water (2×200 ml), brine (100 ml), and dried (MgSO4). The crude was passed through a plug of silica gel with EtOAc providing the desired product 9.2 g (96%) as a 4:1 mixture of cis:trans. MS calculated for C10H12BrNS−H 367, observed M-tBu 309, 311, 313.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07981919B2 |
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| 出典データセット | uspto-grants-2011_07 |
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| ORD ID | ord-d3adc91749404b14862e10decbf7c051 |
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| 出典メモ | uspto-grants-2011_07 |
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