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HRID 30297作成日:2026年10月26日

18-Crown-6 → 3-Benzo[b]thiophen-2-yl-acrylic acid tert-butyl ester

https://huagongshe.com/reaction/30297

反応式

関与物質

役割名称HCID仕込み量
反応物18-Crown-6HCID 28557—
反応物1-Benzothiophene-2-carbaldehydeHCID 736500—
反応物Potassium bis(trimethylsilyl)amideHCID 3251421—
反応物Tert-butyl (diphenoxyphosphoryl)acetateHCID 10689048—
溶媒TetrahydrofuranHCID 8028—
生成物3-Benzo[b]thiophen-2-yl-acrylic acid tert-butyl esterHCID 6720586774.3%

反応手順

Potassium bis(trimethylsilyl)amide (5.4 g, 0.027 mol) was added to a solution of 18-Crown-6 (13.7 g, 0.052 mol) and (diphenoxy-phosphoryl)-acetic acid tert-butyl ester (9.4 g, 0.027 mol) in dry THF (120 mL) at −780C. After 30 minutes of stirring at this temperature, benzo[b]thiophene-2-carbaldehyde (4.0 g, 0.024 mol) was added and the reaction was stirred for 3 hours at −780C after which the reaction was quenched with saturated ammonium chloride (200 mL). The reaction mix was allowed to come to room temperature and was extracted with ethyl acetate (3×200 mL) and the combined organic extracts were washed with 10% HCl (200 mL), brine (200 mL), and dried over MgSO4. The solvent was evaporated in vacuo leaving the crude product that was purified by column chromatography (SiO2) using a 5-40% ethylacetate-hexane gradient to afford the subtitle compound (4.64 g, yield: 74%). MS calculated for C15H16O2S+H: 261, observed: 261.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423056B2
出典データセットuspto-grants-2008_09
ORD IDord-12dd5bc21924475c9ca1463e88122183
出典メモuspto-grants-2008_09