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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 857076생성일: 2026년 10월 24일

Water → 8-(2-Benzothiazolyl)-1,4-dioxaspiro[4.5]decan-8-ol

https://huagongshe.com/ko/reaction/857076

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물BenzothiazoleHCID 7222—
반응물1,4-Dioxaspiro[4.5]decan-8-oneHCID 567415—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물8-(2-Benzothiazolyl)-1,4-dioxaspiro[4.5]decan-8-olHCID 11087581—

반응 단계

To benzothiazole (3.46 g, 25.6 mmol) dissolved in dry THF under a nitrogen atmosphere at −78° C. was added butyl lithium (17.1 mL of 1.5M solution, 1 equiv.) dropwise. The reaction mixture was stirred for 1 h then 1,4-cyclohexanedione mono-ethylene ketal dissolved in dry THF (15 mL) in one portion. The reaction mixture was stirred at −78° C. for a further 3 h then water (10 mL) was added. The mixture was warmed to room temperature and the white precipitate was collected on a filter, washed with water (2×20 mL) then dried under vacuum to give 4-(benzothiazol-2-yl)-1,1-ethylenedioxy-4-hydroxycyclohexane. The yield was 4.403 g (59%); mp 165° C.; 1H NMR (CDCl3) δ 8.05 (1H, m, benzothiazole H-4/7), 7.89 (1H, m, benzothiazole H-4/7), 7.47 (1H, m, benzothiazole H-5/6), 7.39 (1H, m, benzothiazole H-5/6), 4.02 (4H, s, ethylene 2×CH2), 3.16 (1H, s, OH), 2.41–2.31 (4H, m, cyclohexanone 2×CH2), 1.82–1.72 (4H, m, cyclohexanone 2×CH2); IR (KBr disc) 2897, 1501, 1437, 1368, 1038, 997, 764 cm−1; MS (AP+) 292 (M++1), 274 (M++1-H2O); Anal. (C15H17NO3) C, H, N.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07144893B2
출처 데이터셋uspto-grants-2006_12
ORD IDord-a2c330e36f5849ab9624cb0c9eb28174
출처 메모uspto-grants-2006_12