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HRID 1013359作成日:2026年10月25日

4,5-Dibromothiophene-2-carbaldehyde → cis-3-(4,5-Dibromo-thiophen-2-yl)-acrylic acid tert-butyl ester

https://huagongshe.com/reaction/1013359

反応式

関与物質

役割名称HCID仕込み量
反応物4,5-Dibromothiophene-2-carbaldehydeHCID 813164—
反応物Tert-butyl (diphenoxyphosphoryl)acetateHCID 10689048—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
生成物cis-3-(4,5-Dibromo-thiophen-2-yl)-acrylic acid tert-butyl esterHCID 67205492—

反応条件

温度-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07981919B2
出典データセットuspto-grants-2011_07
ORD IDord-d3adc91749404b14862e10decbf7c051
出典メモuspto-grants-2011_07