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HRID 1024486생성일: 2026년 10월 24일

Acetic Acid → N-(9-chloro-3,4-dihydro-2H-1,5-benzodioxepin-7-ylmethyl)-2-methylpropan-1-amine

https://huagongshe.com/ko/reaction/1024486

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물IsobutylamineHCID 6558—
반응물9-chloro-3,4-dihydro-2H-1,5-benzodioxepine-7-carbaldehydeHCID 4962246—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매1,2-DichloroethaneHCID 11—
생성물N-(9-chloro-3,4-dihydro-2H-1,5-benzodioxepin-7-ylmethyl)-2-methylpropan-1-amineHCID 43087680—

반응 단계

To an ice cold mixture of 9-chloro-3,4-dihydro-2H-1,5-benzodioxepine-7-carbaldehyde (2.07 g) and of isobutylamine (7.5 ml 8 eq.) were combined in 1,2-dichloroethane (75 ml) and cooled in ice water bath. Acetic acid (5.68 ml) was then added and followed by sodium triacetoxyborohydride (2.75 g, 1.4 eq.). The mixture was allowed to stir at room temperature overnight. It was partitioned with aqueous K2CO3 (75 mL, 1.5M). The aqueous layer was extracted with of dichloromethane (75 ml×2). The organic layers were combined, washed with brine, dried over sodium sulfate, and concentrated. The residue was purified by flash column chromatography (10-100% ethyl acetate in hexanes) gave the desired amine as a light yellow oil: MS (m+1)=270.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08722896B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-aec57fd526534ee0a281ac98e20cf341
출처 메모uspto-grants-2014_05