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HRID 458565作成日:2026年10月25日

Ethyl bromoacetate → 14738-27-3

https://huagongshe.com/reaction/458565

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4-MethylbenzenethiolHCID 7811—
反応物Sodium hydrideHCID 24758—
溶媒TetrahydrofuranHCID 8028—
生成物14738-27-3HCID 27149299%

反応手順

A solution of 4-methylbenzenethiol (5 g, 40.25) in dry THF was added dropwise to a suspension of NaH (60% in mineral oil, 1.98 g, 48.30) in THF at room temperature and stirred for 30 min. under N2 atmosphere. Ethylbromoacetate (4.9 mL, 44.27) was added slowly to this solution and further stirred at room temperature for 3 h. The solvent was removed under vacuum. The residue was dissolved in dil. HCl and extracted by ethylacetate. The combined organic phase was washed successively with saturated NaHCO3 solution, water and brine then dried over Na2SO4. Evaporation of organic phase yielded 8.46 g (99%) colorless oil. 1H NMR (CDCl3): δ 1.22 (t, J=7.2 Hz, 3H), 2.32 (s, 3H), 3.57 (s, 2H), 4.14 (q, J=7.2 Hz, 2H), 7.11 (d, J=8.0 Hz, 2H), 7.33 (d, J=8.0 Hz, 2H). EIMS m/z 210 (M+1), 233 (M+23).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07192955B2
出典データセットuspto-grants-2007_03
ORD IDord-e8468486339c4fb995e2f9a8f4c52464
出典メモuspto-grants-2007_03