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HRID 2422213作成日:2026年10月24日

Ethyl bromoacetate → Ethyl 2-(4-methoxyphenyl)sulfanylacetate

https://huagongshe.com/ja/reaction/2422213

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl bromoacetateHCID 7748—
反応物TetrahydrofuranHCID 8028—
反応物TriethylamineHCID 8471—
反応物4-MethoxybenzenethiolHCID 12765—
溶媒EthanolHCID 702—
生成物Ethyl 2-(4-methoxyphenyl)sulfanylacetateHCID 148237192%

反応手順

To an ice-cooled mixture of 4-methoxythiophenol (15 g, 0.11 mol), triethylamine (28 mL, 0.20 mol) and tetrahydrofuran (150 mL) was added ethyl bromoacetate (21 g, 0.13 mol), and the mixture was stirred overnight at room temperature. Ethanol (10 mL) was added, the solvent was evaporated under reduced pressure, and the residue was partitioned between ethyl acetate and water. The organic layer was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=10:1) to give title compound (22 g, yield 92%). oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07960369B2
出典データセットuspto-grants-2011_06
ORD IDord-42d83b6449764e33977a6b0946c3f50d
出典メモuspto-grants-2011_06