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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 746040생성일: 2026년 10월 27일

Dimethyl Sulfoxide → 2,6-Dichloro-4-nitrobenzaldehyde

https://huagongshe.com/reaction/746040

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물TriethylamineHCID 8471—
반응물Oxalyl chlorideHCID 65578—
반응물(2,6-Dichloro-4-nitrophenyl)methanolHCID 23311409—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물2,6-Dichloro-4-nitrobenzaldehydeHCID 21838835—

반응 단계

A solution of dimethyl sulphoxide (1.2 cm3) in dichloromethane (5 cm3) was added dropwise to a stirred solution of oxalyl chloride (0.7 cm3, 8.0 mmol) in dichloromethane (12 cm3) at -60° C. under nitrogen. After 10 mins at -60° C. a solution of 2,6-dichloro-4-nitrobenzylalcohol (1.53 g, 6.9 mmol) in dichloromethane (10 cm3) was added dropwise and the stirred mixture kept at -60° C. for 0.5 h. Triethylamine (4.6 cm3, 33 mmol) was then added and the mixture was allowed to warm to room temperature at which stage water (35 cm3) was added. The heterogeneous mixture was separated and the aqueous phase extracted with dichloromethane (35 cm3). The combined organic fractions were extracted with hydrochloric acid (2M, 60 cm3), then water (60 cm3), saturated sodium carbonate solution (60 cm 3), and finally water (60 cm3) then dried and evaporated under reduced pressure to give 2,6-dichloro-4-nitrobenzaldehyde as a pure oil which slowly solidified.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04602041
출처 데이터셋uspto-grants-1986_07
ORD IDord-5c34ea4784db4b95bab3b91e2d6a1307
출처 메모uspto-grants-1986_07