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Hydrochloric Acid → 2-(2-Oxopyridin-1(2H)-yl)propanoic acid

HRID 243696
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HRID 243696 반응식
[O:1]=[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:3]1[CH:8]([CH3:16])[C:9]([O:11]C(C)(C)C)=[O:10].Cl>O1CCOCC1>[O:1]=[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:3]1[CH:8]([CH3:16])[C:9]([OH:11])=[O:10]
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참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 57907642tert-butyl 2-(2-oxopyridin-1(2H)-yl)propanoate

생성물 1

HCID 167879002-(2-Oxopyridin-1(2H)-yl)propanoic acid수율 99.7%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매2회

실험 절차

To a stirred suspension of 16.6 g (74.4 mmol) of tert-butyl 2-(2-oxopyridin-1(2H)-yl)propanoate from step A above in 10 mL of anhydrous 1,4-dioxane under an atmosphere of nitrogen was added 150 mL of a 4.0 M hydrogen chloride solution in 1,4-dioxane. The resulting solution was stirred overnight at ambient temperature then evaporated to dryness in vacuo to afford the title compound as a white solid (12.4 g, quantitative yield). LC-MS: m/z (ES) 168 (MH)+

후처리

  1. customthen evaporated to dryness in vacuo

출처 및 근거

ORD 기록
ord-13a6dc450395414286736b501ce80caf
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08653260B2

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