돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 399725생성일: 2026년 10월 26일

Trifluoroacetic acid → 3-Methyl-3(2,4,6-trimethoxyphenylmethylthio)butyric acid

https://huagongshe.com/reaction/399725

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물2,4,6-Trimethoxybenzyl alcoholHCID 602515—
반응물3-Methyl-3-sulfanylbutanoic acidHCID 9812786—
용매DichloromethaneHCID 6344—
생성물3-Methyl-3(2,4,6-trimethoxyphenylmethylthio)butyric acidHCID 1545813970%

반응 단계

To a solution of 3-mercapto-3-methylbutyric acid (B. J. Sweetman et al. J. Med Chem., 14, 868 (1971)) (4.6 g, 34 mmol) in methylene chloride (250 mL) under nitrogen and cooled over ice/salt to 5 uC (internal temperature) was added trifluoroacetic acid (82 g, 0.72 mol). No significant temperature rise was noted during the addition. To this was then added dropwise a solution of 2,4,6-trimethoxybenzyl alcohol (M. C. Munson et al., J. Org. Chem., 57, 3013 (1992)) (6.45 g, 32 mmol) in methylene chloride (150 mL) such that the reaction temperature does not rise above 5 uC. After the addition was complete, the mixture was stirred for an additional 5 min at 5 uC and the volatiles were removed in vacuo (toluene or ethyl acetate can be used to assist in the removal of volatile material). The residue was partitioned between diethyl ether and water and the organic phase dried over anhydrous sodium sulfate, filtered and the volatile material removed in vacuo. The residue was treated with activated charcoal and recrystalised from diethyl ether/hexane. The product was isolated as an white solid in 70% yield (7 g) mp 103°-105° C. 1H NMR (CDCl3) δ 6.12 (s, 2 H), 3.80-3.85 (m, 11 H), 2.74 (s, 2 H), 1.47 (s, 6 H). 13C NMR (CDCl3) δ 173.9, 160.6, 158.6, 105.6, 90.5, 55.7, 55.3, 45.9, 43.6, 28.4, 21.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05824669
출처 데이터셋uspto-grants-1998_10
ORD IDord-bfd11097353d46c4a13d5a53a8a41048
출처 메모uspto-grants-1998_10