돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1730813생성일: 2026년 10월 25일

Triethylamine → N-cyclopentyl-2-methylfuran-3-hydroxamic acid

https://huagongshe.com/reaction/1730813

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-Methylfuran-3-carbonyl chlorideHCID 2759850—
반응물N-cyclopentylhydroxylamine hydrochlorideHCID 21496528—
용매BenzeneHCID 241—
생성물N-cyclopentyl-2-methylfuran-3-hydroxamic acidHCID 21496529—

반응 단계

30 Parts of triethylamine is added to a suspension of 20 parts of N-cyclopentylhydroxylamine hydrochloride in 300 parts of benzene and the whole is stirred for 1 hour. At room temperature, 10 parts of 2-methylfuran-3-carboxylic chloride is dripped in. After the mixture has been stirred for a further 3 hours it is suction filtered, the residue is washed with benzene, and the organic phase is washed with water, dried with sodium sulfate and evaporated. There is obtained 25 parts of N-cyclopentyl-2-methylfuran-3-hydroxamic acid in the form of an oil. This oil is dissolved in 300 parts of dichloromethane; while stirring and at room temperature, 16 parts of sodium hydroxide in 70 parts of water, and 26 parts of dimethyl sulfate are added to the solution. After the mixture has been stirred for 2 hours the organic phase is separated, washed with water until neutral and dried with anhydrous sodium sulfate. Distillation gives 21 parts of O-methyl-N-cyclopentyl-2-methylfuran- 3-hydroxamic acid having a boiling point at 0.01 mm Hg of 104° to 108° C and the refractive index nD25 : 1.5073. ##SPC14##

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03993772
출처 데이터셋uspto-grants-1976_11
ORD IDord-fde7138661a444c3a0850e0d1c477f10
출처 메모uspto-grants-1976_11