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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1046438생성일: 2026년 10월 26일

Dimethyl Sulfoxide → 2,2-Dimethyl-3-((tetrahydro-2H-pyran-2-yl)oxy)propanal

https://huagongshe.com/reaction/1046438

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물TriethylamineHCID 8471—
반응물Ammonium ChlorideHCID 25517—
반응물Oxalyl chlorideHCID 65578—
반응물2,2-Dimethyl-3-(tetrahydro-pyran-2-yloxy)-propan-1-olHCID 15811365—
용매DichloromethaneHCID 6344—
생성물2,2-Dimethyl-3-((tetrahydro-2H-pyran-2-yl)oxy)propanalHCID 1327645897.7%

반응 조건

온도-78 °C

반응 단계

DMSO (2.69 mL, 50.97 mmol) was added dropwise to a solution of oxalyl chloride (2.87 mL, 33.98 mmol) in dichloromethane (85.0 mL) at −78° C. After several minutes, neat 2,2-dimethyl-3-(tetrahydro-pyran-2-yloxy)-propan-1-ol (3.2 g, 16.99 mmol) was added dropwise and after stirring for 1 h at −78° C., triethylamine (9.5 mL, 68.0 mmol) was added. The reaction was allowed to warm to room temperature and stirred for 30 min. Sat. NH4Cl was added and the organic layer was separated. The aqueous layer was extracted with ethyl acetate and washed with brine. The organic layers were combined, dried over Na2SO4 and concentrated to give a pale liquid. The crude liquid was passed through a short silica gel column and eluted with 50% ethyl acetate in hexanes to provide 2,2-dimethyl-3-(tetrahydro-pyran-2-yloxy)-propionaldehyde (3.09 g, 97%) as a pale liquid after removal of solvents under reduced pressure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08569302B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-20da1a9063e842bd9d058a0d784b622f
출처 메모uspto-grants-2013_10