돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1781216생성일: 2026년 10월 26일

Mercaptoethanesulfonic acid → 1,1,4,4-Tetramethyltetralin

https://huagongshe.com/reaction/1781216

반응식

참여 물질

역할이름HCID투입량
반응물Mercaptoethanesulfonic acidHCID 598—
반응물Potassium CarbonateHCID 11430—
반응물2-Bromo-1-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)ethan-1-oneHCID 2801337—
반응물SodiumHCID 5360545—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물1,1,4,4-TetramethyltetralinHCID 81186—
생성물SodiumHCID 5360545—

반응 단계

To a solution of 6-(bromoacetyl)-1,2,3,4-tetrahydro-1,1,4,4-tetramethylnaphthalene (12) (15.5 mg, 0.050 mmol) in DMF (0.13 mL) and THF (0.13 mL) was added a freshly prepared solution of 2-mercapto-1-ethanesulfonic acid, sodium salt (2) (25 mg, 0.15 mmol) and potassium carbonate (21 mg, 0.15 mmol) in water (0.15 mL) at room temperature. The resulting biphasic mixture was stirred for 30 min. The reaction mixture was diluted with ethyl acetate (2.5 mL), and the organic layer was separated, washed with water (2×1 mL) and brine (1×1 mL), dried and concentrated to afford 6-[2'-mercapto-1'-ethanesulfonic acid, sodium salt)acetyl]-1,2,3,4-tetrahydro-1,1,4,4-tetramethylnaphthalene (20) as a solid. 1H NMR (pyr-d5): δ 8.19, 7.90, 7.40 (m, 3H), 4.11 (s, 2H), 3.5 (m, 4H), 1.55 (s, 4H), 1.20 (d, 12H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05632898
출처 데이터셋uspto-grants-1997_05
ORD IDord-bd07e98aceef4b509d4e39b6ba9624c9
출처 메모uspto-grants-1997_05