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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 65067생성일: 2026년 10월 24일

Carbon Disulfide → n-Hexyl (3S)-3-hydroxymethyl-1,2,3,4-tetrahydro-beta-carboline-2-carbodithioate

https://huagongshe.com/ko/reaction/65067

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DisulfideHCID 6348—
반응물1-BromohexaneHCID 8101—
반응물TriethylamineHCID 8471—
반응물(3S)-3-hydroxymethyl-1,2,3,4-tetrahydro-beta-carbolineHCID 13375506—
용매Dimethyl SulfoxideHCID 679—
생성물n-Hexyl (3S)-3-hydroxymethyl-1,2,3,4-tetrahydro-beta-carboline-2-carbodithioateHCID 1339298173.2%

반응 단계

(3S)-3-Hydroxymethyl-1,2,3,4-tetrahydro-β-carboline (2.02 g) is dissolved in dimethylsulfoxide (10 ml), and thereto are added triethylamine (1.67 ml) and CS2 (0.72 ml), and the mixture is stirred at room temperature for 20 minutes. To the reaction mixture is added dropwise n-hexyl bromide (1.98 g), and the mixture is stirred at room temperature for 2.5 hours. The reaction mixture is poured onto ice-water and the mixture is extracted with ethyl acetate. The ethyl acetate layer is washed with water, dried over sodium sulfate, and then distilled to remove the solvent. The residue is recrystallized from ether-n-hexane to give the title compound (2.65 g, 73.2%) as colorless needles, m.p. 102°-106° C. NMR (CDCl3, δ): 0.90 (broad, t, 3H, --(CH2)5 --CH3); Mass m/e: 362 (M+), 244 (M+ --C6H13SH); [α]D20 +130.0° (c=1.0, methanol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04612317
출처 데이터셋uspto-grants-1986_09
ORD IDord-537bca8a081e45dbbc8a50af57fc05e0
출처 메모uspto-grants-1986_09