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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1995478생성일: 2026년 10월 24일

Hydroxylamine → 3-chloro-N-(2-chlorophenyl)methyl-N-hydroxy-2,2-dimethylpropanamide

https://huagongshe.com/ko/reaction/1995478

반응식

참여 물질

역할이름HCID투입량
반응물HydroxylamineHCID 787—
반응물PyridineHCID 1049—
반응물3-Chloro-2,2-dimethylpropanoyl chlorideHCID 61345—
반응물N-(2-ChlorobenZyl)hydroxylamineHCID 12811040—
용매DichloromethaneHCID 6344—
용매HexaneHCID 8058—
생성물3-chloro-N-(2-chlorophenyl)methyl-N-hydroxy-2,2-dimethylpropanamideHCID 992555820.6%

반응 단계

Under an argon atmosphere a stirred solution of 10.2 grams (0.065 mole) of N-(2-chlorophenylmethyl)hydroxylamine and 6.1 grams (0.077 mole) of pyridine in 80 ml of methylene chloride was cooled to -10°. A solution of 10.0 grams (0.065 mole) of 3-chloro-2,2-dimethylpropionyl chloride in 20 ml of methylene chloride was added dropwise to the hydroxylamine solution during a 20 minute period. Upon completion of addition the reaction mixture was allowed to warm to ambient temperature where it was stirred for 16 hours. The reaction mixture was diluted with 100 ml of methylene chloride and washed with 100 ml of water, 100 ml of aqueous 10% hydrochloric acid, and finally 100 ml of water. The organic layer was dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure to give a residual oil. The oil was taken up in 25 ml of hexane and cooled in an icewater bath. The resultant solid precipitate was collected by filtration and recrystallized from hexaneethyl acetate to give 3.7 grams of 3-chloro-N-(2-chlorophenyl)methyl-N-hydroxy-2,2-dimethylpropanamide; mp 108°-110°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04405357
출처 데이터셋uspto-grants-1983_09
ORD IDord-0c2423f1d30746a181de50d52efac4f5
출처 메모uspto-grants-1983_09