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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 443827생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/443827

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrothiopheneHCID 1127—
반응물Methyl AnthranilateHCID 8635—
반응물Tert-Butyl hypochloriteHCID 521297—
반응물N-chloroanthranilateHCID 23465897—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물Methyl 2-amino-3-(tetrahydro-2-thienyl)benzoateHCID 12713254—

반응 단계

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°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04261996
출처 데이터셋uspto-grants-1981_04
ORD IDord-9fdd77b5cd204c609ca3cebe824ff70c
출처 메모uspto-grants-1981_04