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tert-Butoxy bis(dimethylamino)methane → HCID 74828433, 화합물

HRID 2236887
노트
인쇄 미리보기

반응식

HRID 2236887 반응식
[O:1]1[CH:5]=[CH:4][C:3]([N:6]2[CH:11]=[CH:10][C:9]([CH3:12])=[CH:8][C:7]2=[O:13])=[CH:2]1.C(O[CH:19](N(C)C)[N:20]([CH3:22])[CH3:21])(C)(C)C>CN(C)C=O>[CH3:19][N:20]([CH3:22])[CH:21]=[CH:12][C:9]1[CH:10]=[CH:11][N:6]([C:3]2[CH:4]=[CH:5][O:1][CH:2]=2)[C:7](=[O:13])[CH:8]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 79885tert-Butoxy bis(dimethylamino)methaneHCID 426257441-(3-Furanyl)-4-methyl-2(1H)-pyridinone

생성물 1

HCID 74828433HCID 74828433, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
150 °C

실험 절차

A mixture of 1-furan-3-yl-4-methyl-1H-pyridin-2-one (3.7 g, 21 mmol), tert-butoxybis(dimethylamino)methane (11 g, 63 mmol), and N,N-dimethylformamide (4 mL) is heated in a 150° C. oil bath for 2½ hours and then concentrated to dryness under reduced pressure. A quantitative yield of 4-(2-dimethylamino-vinyl)-1-furan-3-yl-1H-pyridin-2-one is assumed, and the material is carried on without further purification.

후처리

  1. concentrationconcentrated to dryness under reduced pressure

출처 및 근거

ORD 기록
ord-aa02f9eba6284554836aa904a4ef6aa0
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07713994B2

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