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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1440341생성일: 2026년 10월 26일

Formaldehyde → 3-{2-(1-Pyrrolidinylmethyl)-butyryl}-1,2-benzisoxazole

https://huagongshe.com/reaction/1440341

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물PyrrolidineHCID 31268—
반응물Sodium BicarbonateHCID 516892—
반응물3-Butyryl-1,2-benzisoxazoleHCID 19976921—
용매EthanolHCID 702—
용매Ethyl AcetateHCID 8857—
생성물3-{2-(1-Pyrrolidinylmethyl)-butyryl}-1,2-benzisoxazoleHCID 19976943—

반응 단계

Added to 10 ml of ethanol were 1.55 g (8.2 mmol) of 3-butyryl-l,2-benzisoxazole prepared above in the procedure (1), 0.52 ml (9.9 mmol) of a 37% aqueous solution of formaldehyde and 0.82 ml (9.8 mmol) of pyrrolidine. The resultant mixture was heated under reflux for 3 hours. After cooling, the solvent was distilled off. The residue thus obtained was added to 50 ml of ethyl acetate, followed by extraction with 50 ml of dilute hydrochloric acid. A water layer thus obtained was alkalinized with an aqueous solution of sodium hydrogencarbonate, followed by extraction with 50 ml of ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and the solvent was then distilled off, whereby 3-{2(1-pyrrolidinylmethyl)butyryl}-1,2-benzisoxazole was obtained as oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05498619
출처 데이터셋uspto-grants-1996_03
ORD IDord-175eaccd88414ee59468c260c60c0312
출처 메모uspto-grants-1996_03