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HRID 443827作成日:2026年10月26日

Tetrahydrothiophene → Methyl 2-amino-3-(tetrahydro-2-thienyl)benzoate

https://huagongshe.com/reaction/443827

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrothiopheneHCID 1127—
反応物Methyl AnthranilateHCID 8635—
反応物Tert-Butyl hypochloriteHCID 521297—
反応物N-chloroanthranilateHCID 23465897—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
生成物Methyl 2-amino-3-(tetrahydro-2-thienyl)benzoateHCID 12713254—

反応手順

A solution of methyl anthranilate (75.5 g; 0.5 mole) in CH2Cl2 (1.0 l) is cooled to -70° and a solution of tert-butyl hypochlorite (54 g; 0.5 mole) in CH2Cl2 (150 ml) is added slowly keeping the temperature at -70°. The resultant N-chloroanthranilate solution is stirred for 1.0 hr and then tetrahydrothiophene (110 ml) is added at such a rate as to maintain the exotherm to less than 10°. The dark solution is stirred at -70° for 2.0 hr, triethylamine (125 ml) is added dropwise, and the solution is stirred for 24 hrs. The solvents are removed and the residue is diluted with CH2Cl2, washed with (1 N) NaOH solution, water and dried. Removal of solvents gives an oil. Unreacted methyl anthranilate is removed under reduced pressure (b.p. 95°-100°/0.35 mm) at bath temperature at 150°. The residue is dissolved in CH 2 Cl2 and partially chromatographed through silica gel. The solid residue is recrystallized from methanol. Yield 27.0 g; mp 75°-9°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04261996
出典データセットuspto-grants-1981_04
ORD IDord-9fdd77b5cd204c609ca3cebe824ff70c
出典メモuspto-grants-1981_04