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Hydrochloric Acid → HCID 22170131, 화합물

HRID 1823279
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HRID 1823279 반응식
C([O:3][C:4]([C:6]1[C:7]([C:12]2[CH:13]=[N:14][CH:15]=[CH:16][C:17]=2[Cl:18])=[N:8][O:9][C:10]=1[CH3:11])=[O:5])C.[OH-].[Na+].C(O)C.Cl>O1CCCC1>[Cl:18][C:17]1[CH:16]=[CH:15][N:14]=[CH:13][C:12]=1[C:7]1[C:6]([C:4]([OH:5])=[O:3])=[C:10]([CH3:11])[O:9][N:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 702EthanolHCID 14798Sodium HydroxideHCID 574254393-(4-Chloro-pyridin-3-yl)-5-methyl-isoxazole-4-carboxylic acid ethyl ester

생성물 1

HCID 22170131HCID 22170131, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

Combine 3-(4-chloro-pyridin-3-yl)-5-methyl-isoxazole-4-carboxylic acid ethyl ester (0.90 g, 0.003 mol) with aqueous sodium hydroxide (2N, 7.0 mL, 0.014 mol), ethanol (2 mL), and tetrahydrofuran (2 mL) and stir overnight at ambient temperature. Adjust the aqueous mixture to approx. pH 2.5 with aqueous hydrochloric acid. Extract with ethyl acetate and dry the combined extracts over sodium sulfate and concentrate in vacuo. Drying nets the desired isoxazole acid as a light solid (0.78 g, 97%). MS(ES): (M+1)+ 239.0, 241.0 m/z.

후처리

  1. extractionExtract with ethyl acetate
  2. dry with materialdry the combined extracts over sodium sulfate
  3. concentrationconcentrate in vacuo
  4. customDrying

출처 및 근거

ORD 기록
ord-d8ed08fa0aeb4f4586e1f0ff9706dcec
출처 데이터셋
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07037921B2

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